Method for forming a mesh having a barbed suture attached thereto and the mesh thus obtained

- SOFRADIM PRODUCTION

The invention relates to a method for forming a mesh having a barbed suture attached thereto, comprising the following steps: a) producing a knitted structure on a knitting machine comprising at least one needle-bed with three guide bars, on a length corresponding to N stitches ranging from 1 to N, wherein i) a first knit portion is produced along stitches ranging from 1 to x, where 1<x<N, ii) a second knit portion is produced for stitches ranging from (x+1) to N, in which the knitting pattern produces at least one weft stitched chain stitch, b) cutting the second knit portion on both sides of the weft stitched chain stitch and along an edge separating the second knit portion from the first knit portion, while maintaining the weft stitched chain stitch attached to the first knit portion. The invention also relates to the mesh obtained by this method.

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Description
CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims benefit of and priority to European Patent Application No. 16306383.7 filed Oct. 21, 2016, the disclosure of the above-identified application is hereby incorporated by reference in its entirety.

BACKGROUND OF THE INVENTION

The present invention relates to a method for forming a prosthetic mesh having one or more barbed suture(s) attached thereto, such a prosthetic mesh being useful in the surgical field. The method of the invention allows producing a prosthetic mesh having one or more barbed suture(s) attached thereto in a reduced time and in a very cost-effective way.

The abdominal wall in humans is composed of fat and muscles interconnected by fascias. It sometimes happens that a break in continuity occurs in the fascias, allowing part of the peritoneum to slip through and form a sac, or a hernia, containing either fat or part of the intestines. Hernias or incisional hernias (a hernia occurring through a parietal surgical scar) show themselves in the form of a bulge at the surface of the skin and are classed, for example, as umbilical or inguinal hernias or incisional hernias, depending on where they are located.

In order to repair a hernia defect, surgeons often fit a prosthesis in place which is made of synthetic mesh and replaces or strengthens the weakened anatomical tissues.

Within the meaning of the present application, a “mesh” is understood as an arrangement of biocompatible yarns, such as a textile or fabric, preferably open-worked, that is to say provided with pores that favour recolonization of tissue such as cellular growth. Such a mesh can be bioresorbable, permanent or partially bioresorbable. It is sufficiently flexible to be folded up at the time of introduction into the abdominal cavity.

Meshes for forming hernia prosthesis are well known to a person skilled in the art. The mesh can be supplied in any shape whatsoever, for example rectangular, square, circular, oval, etc., and can then be cut to suit the shape of the hernia defect. For example, the overall shape of the mesh can be circular or oval. Alternatively, the mesh can have a generally square shape or a rectangular shape.

Meshes for forming hernia prosthesis are advantageously provided as a knitted structure obtained with biocompatible yarns. Knitting methods allow obtaining knitted structure having openworked faces that promote cell recolonization after implantation.

Once implanted, the mesh must be fixed to the surroundings biological tissues, such as for example the abdominal wall. Many fixing means are available for fixing the mesh to the abdominal wall, such as tacks, staples, adhesives or sutures.

The use of sutures usually imply forming surgical knots in order to anchor the suture.

Surgical knots have been used for ages in order to anchor and allow a conventional suture, in other words a smooth suture without barbs, to perform its role in mesh fixation for example. Anyway, surgical knots reduce the tensile strength of conventional sutures by thinning and stretching the material forming the suture. Indeed, it is known that the weakest portion of any suture line is the knot.

Moreover, the tying of surgical knots introduces the potential of human error. A knot-secured conventional suture may create an uneven distribution of tension across the wound, with the higher tension burden placed at the knots. In addition, in minimally invasive laparoscopic surgery, the ability to quickly and properly tie surgical knots presents a challenge. The skill necessary for performing intra- or extracorporeal knot tying for laparoscopic surgery may be acquired only with practice and patience, yet surgeons need to master such a skill in order to properly perform closure procedures. Laparoscopic knot tying is also more mentally and physically stressful on surgeons.

Given the excessive relative wound tension on the knot and the reasonable concerns of surgeons for suture failure due to knot slippage, there is a natural tendency toward overcoming these potential issues by over-tightening knots. However, tighter knots may be worse for wound healing and strength than looser knots. Surgical knots, when tied too tightly, can cause localized hypoxia, reduced fibroblast proliferation, and excessive tissue overlap, leading to reduced strength in the healed wound.

Eventually, a surgical knot yields the highest density of foreign body material in any given suture line and the volume of a knot may be directly related to the total amount of surrounding inflammatory reaction. If minimizing the inflammatory reaction in a wound is important for optimized wound healing, then minimizing knots sizes or even eliminating knots altogether would be beneficial as long as the wound-holding strength of the suture line is not compromised.

For all these reasons, the use of barbed suture, suture with barbs, has tremendously increased in the past years. In particular, one of the most costly parts of a surgical procedure is time in the operating room.

Barbed sutures are known. They basically consist in strands of smooth suture provided with barbs on their surfaces. Barbed sutures are generally made of the same materials as conventional sutures and offer several advantages for fixing meshes to the abdominal wall compared with conventional sutures. A barbed suture includes an elongated body that has one or more spaced barbs, that project from the surface of the suture body along the body length.

The barbs are generally arranged to allow passage of the barbed suture in one direction through tissue but resist movement of the barbed suture in the opposite direction (one-way suture). One advantage of barbed sutures is the provision of a non-slip property.

Barbed sutures are known for use in laparoscopic and endoscopic procedures. The number of barbs needed for a particular suture may be influenced by the size of the wound and the strength required to fix the mesh. Like a conventional suture, a barbed suture may be inserted into tissue using a surgical needle.

In some circumstances, a random configuration of barbs on the exterior surface of the suture is preferred to achieve optimal fixing of the mesh. However, in other circumstances, where the tissue repair needed is relatively small, a reduced number of barbs may be desired.

Various methods of forming barbs on sutures have been proposed such as mechanical cutting, laser cutting, injection molding, stamping, extrusion and the like. However, such methods may be difficult or costly, in particular when a specific arrangement or configuration of barbs is needed for an appropriate surgical procedure.

For example, conventional cutting methods of forming barbs may involve cutting with a blade into the elongate body of the suture, where the elongate body may be a monofilament for example. Barbed sutures may be fabricated from monofilament fibers by a micro-machining technique, which escarpes barbs into the fiber around the circumference in a variety of configurations. Cutting methods have therefore significant drawbacks as they weaken the core of the suture and narrow its functional diameter. Moreover, they are costly and have slow manufacturing cycle time.

Accordingly, there is a continuous need for methods of forming barbs on a suture that are less difficult to implement, more efficient and cost effective. There is also a continuous need for methods allowing varying the size, the location and the depth of the barbs, as well as the amount of barbs present on the suture, depending on the contemplated surgical application.

In particular, there is a need for providing a mesh having one or more barbed suture(s) attached thereto, so that the surgeon does not have to waste time looking for a suture at the time he needs to fix the mesh to the biological tissue during the implantation.

A first aspect of the invention is a method for forming a prosthetic mesh having at least a barbed suture attached thereto, said barbed suture comprising an elongate body provided with barbs extending substantially radially out from said elongate body, said method comprising the following steps:

a) producing a knitted structure on a warp knitting machine comprising at least one needle-bed comprising at least three guide bars, a first guide bar B1, a second guide bar B2 and a third guide bar B3, said first guide bar B1 being threaded with first yarns of a biocompatible material, said second guide bar B2 being threaded with second yarns of a biocompatible material, said third guide bar B3 being threaded with third yarns of a biocompatible material, said knitted structure being produced on a determined length along the warp direction corresponding to a total number of N stitches ranging from 1 to N completed along said warp direction by the machine, N being an integer above 7, wherein

    • i) a first knit portion is produced along stitches ranging from 1 to x, where 1<x<N, in which the knitting patterns followed by the first, the second and the third guide bars (B1, B2, B3) produce an openworked knit capable of favoring cellular growth,
    • ii) a second knit portion is produced for stitches ranging from (x+1) to N, in which the knitting pattern followed by said second and third guide bars (B2, B3) produces chain stitches and the knitting pattern followed by the first guide bar B1 produces at least a partial weft in which said first yarns complete weft stitches with at least one of said chain stitches, thereby producing at least one weft stitched chain stitch,

b) cutting the second knit portion along the warp direction on both sides of said at least one weft stitched chain stitch and along an edge separating the second knit portion from the first knit portion, so as to remove the second knit portion from the knitted structure while maintaining said weft stitched chain stitch attached to the first knit portion,

wherein the first knit portion forms the mesh and the second or third yarn forming part of said at least one weft stitched chain stitch forms said elongate body of said barbed suture attached thereto, the first yarns cuts extending from said weft stitches of said at least one weft stitched chain stitch forming said barbs of said barbed suture.

In the prosthetic mesh obtained by the method of the invention, the barbed suture therefore comprises an elongate body made of a yarn of a biocompatible material coming either from guide bar B2 (second yarn) or from guide bar B3 (third yarn), provided with barbs extending substantially radially out from said elongate body, said barbs being first yarns cuts made of a biocompatible material, where said first yarns cuts are stitched to said second or third yarn forming said elongate body. The first yarn cuts result from the cutting of the second knit portion on both sides of the at least one weft stitched chain stitch. In embodiments, said elongate body(ies) of said barbed suture(s) is/are formed of second yarns only.

In the present application, “N” and “x” correspond to numbers of stitches and are therefore integers.

In the present application, by “knit capable of favoring cellular growth” is meant a knit the knitting pattern of which allows creating voids, pores, channels on the surfaces and/or within the thickness of the knit so that cells may colonize the knit once the knit is implanted in the body of a human being.

Another aspect of the invention is a prosthetic mesh having at least a barbed suture attached thereto, said barbed suture comprising an elongate body made of a yarn of biocompatible material, provided with barbs extending substantially radially out from said elongate body, said barbs being yarns cuts made of a biocompatible material, where said yarns cuts are stitched to said yarn forming said elongate body, said prosthetic mesh being obtained by the method above.

In a first step, step a), of the method of the invention, a knitted structure is produced on a warp knitting machine. The warp knitting machine comprises at least one needle-bed comprising at least three guide bars, a first guide bar B1, a second guide bar B2 and a third guide bar B3. The first guide bar B1 is threaded with first yarns of a biocompatible material, the second guide bar B2 is threaded with second yarns of a biocompatible material, the third guide bar B3 being threaded with third yarns of a biocompatible material. The knitted structure is produced on a determined length along the warp direction corresponding to a total number of N stitches ranging from 1 to N completed along said warp direction by the machine, N being an integer above 7. During this step a), i) a first knit portion is produced along stitches ranging from 1 to x, where 1<x<N, in which the knitting patterns followed by the first, the second and the third guide bars (B1, B2, B3) produce an openworked knit capable of favoring cellular growth, and ii) a second knit portion is produced for stitches ranging from (x+1) to N, in which the knitting pattern followed by said second and third guide bars (B2, B3) produces chain stitches and the knitting pattern followed by the first guide bar B1 produces at least a partial weft in which said first yarns complete weft stitches with at least one of said chain stitches, thereby producing at least one weft stitched chain stitch.

The warp knitting machine may be for example a crochet machine or a raschel knitting machine or a Jacquard machine. Warp knitting machines have a warp yarn for each needle.

By “chain stitch” is meant according to the present application a stitch construction where both over and underlapping are always carried out across the same needle. One chain stitch of a knit therefore involves only one warp yarn, in other words involves only one yarn in the warp direction. The tensile strength of one chain stitch is therefore the tensile strength of said single warp yarn involved in the construction of the chain stitch.

The warp knitting machine may comprise one or more needle-bed(s). For example, the warp knitting machine may comprise two needle-beds. Such double needle-bed machines allow producing bidimensional knits and three-dimensional knits.

In the present application by “bidimensional knit” is meant a knit obtained on a warp knitting machine with the use of one needle-bed only, whatever the number of needle-beds present in the machine, and whatever the number of guide bars present in said one needle-bed. For example, a bidimensional knit may be obtained with two guide bars or more, as long as said guide bars all belong to one needle-bed only. Bidimensional knits may also be obtained on a Jacquard machine, where each guide bar elements are independent.

In the present application by “three-dimensional knit” is meant a knit obtained on a warp knitting machine with the use of two needle-beds, with yarns crossing from a needle-bed to the other.

In embodiments, the warp knitting machine comprises two needle-beds, a first needle-bed comprising said first, second and third guide bars (B1, B2, B3) described above, and a second needle-bed comprising fourth guide bar B4, fifth guide bar B5 and sixth guide bar B6. The fourth guide bar B4 is threaded with fourth yarns of a biocompatible material, the fifth guide bar B5 is threaded with fifth yarns of a biocompatible material, the sixth guide bar B6 is threaded with sixth yarns of a biocompatible material. In such embodiments, the first and second knit portions may be produced by using the six guide bars (B1, B2, B3, B4, B5 and B6).

In such embodiments, step a) may comprise a step 0) occurring before step a)i) as follows:

0) a connecting knit portion is produced along stitches ranging from 1 to y, where 1<y<x<N, in which the knitting patterns followed by first, second, third, fourth, fifth and sixth guide bars (B1, B2, B3, B4, B5, B6) produce a three-dimensional openworked knit capable of favoring cellular growth, said knit having a first face produced on said first needle-bed by said first, second and third yarns from said first, second and third guide bars (B1, B2, B3), and a second face, produced on said second needle-bed by said fourth, fifth and sixth yarns from said fourth, fifth and sixth guide bars (B4, B5, B6), said first and second faces being linked together by some of the second, third, fourth and/or fifth yarns, preferably by some of the third and/or fourth yarns, crossing from the first needle-bed to the second needle-bed and vice-versa, thereby forming linking yarns,

and, in step i), the first knit portion is produced along stitches ranging from (y+1) to x, in which the knitting patterns followed by the first, second and third guide bars (B1, B2, B3) produce on the first needle-bed a first bidimensional openworked knit capable of favoring cellular growth, and in which the knitting patterns followed by the fourth, fifth and sixth guide bars (B4, B5, B6) produce on the second needle-bed a second bidimensional openworked knit capable of favoring cellular growth,

said first and second bidimensional openworked knits being independent from each other,

and, in step ii), the second knit portion is produced for stitches ranging from (x+1) to N, in which:

on said first needle-bed, a first needle-bed second knit portion is produced, in which the knitting pattern followed by said second and third guide bars (B2, B3) produces chain stitches and the knitting pattern followed by the first guide bar B1 produces at least a partial weft in which said first yarns complete weft stitches with at least one of said chain stitches, thereby producing at least one first weft stitched chain stitch,

on said second needle-bed, a second needle-bed second knit portion is produced, in which the knitting pattern followed by said fourth and fifth guide bars (B4, B5) produces chain stitches and the knitting pattern followed by the sixth guide bar B6 produces at least a partial weft in which said sixth yarns complete weft stitches with at least one of said chain stitches, thereby producing at least one second weft stitched chain stitch,

said first needle-bed second knit portion and said second needle-bed second knit portion being independent from each other.

In the present application, “y” corresponds to a number of stitches and is therefore an integer.

In the present application, by “independent knits” with respect to two knits produced, for example simultaneously, on a double-bed knitting machine, is meant one knit produced on the first needle-bed and a second knit produced on the second needle-bed, with no yarns from one needle-bed crossing to the other needle-bed during the production of said two independent knits.

In the present application, the terms “weft stitched chain stitch”, “first weft stitched chain stitch” and “second weft stitched chain stitch” all relate to weft stitched chain stitches obtained according to the method of the invention and generally referred to as “weft stitched chain stitch”, the terms “first weft stitched chain stitch” and “second weft stitched chain stitch” being used for sake of clarity when two needle-beds are used, as it may be useful to distinguish the first weft stitched chain stitches obtained with the first needle-bed from the second weft stitched chain stitches obtained with the second needle-bed.

In embodiments where the warp knitting machine comprises a first needle-bed comprising first, second and third guide bars (B1, B2, B3) and a second needle-bed comprising fourth, fifth and sixth guide bars (B4, B5, B6) as described above, the cutting step bo) may comprise the following steps:

cutting the first needle-bed second knit portion along the warp direction on both sides of said at least one first weft stitched chain stitch and along an edge separating the first needle-bed second knit portion from the first bidimensional openworked knit, so as to remove the first needle-bed second knit portion from the knitted structure while maintaining said first weft stitched chain stitch attached to the first bidimensional openworked knit,

cutting the second needle-bed second knit portion along the warp direction on both sides of said at least one second weft stitched chain stitch and along an edge separating the second needle-bed second knit portion from the second bidimensional openworked knit, so as to remove the second needle-bed second knit portion from the knitted structure while maintaining said second weft stitched chain stitch attached to the second bidimensional openworked knit,

and the method may further comprise the following steps occurring after step bo):

co) optionally cutting said linking yarns from the three-dimensional openworked knit obtained in step a)0) along stitches ranging from 2 to y,

do) opening the knitted structure so as to spread in a single plane the part of the knitted structure obtained from the first needle-bed and the part of the knitted structure obtained from the second needle-bed,

wherein the first bidimensional openworked knit, the connecting knit portion, optionally cut according to step co), and the second bidimensional openworked knit form altogether the mesh; the second or third yarn forming part of said at least one first weft stitched chain stitch forms the elongate body of a first barbed suture attached to the first bidimensional openworked knit, the first yarns cuts extending from said weft stitches of said at least one first weft stitched chain stitch forming said barbs of said first barbed suture; the fourth or fifth yarn forming part of said at least one second weft stitched chain stitch forms the elongate body of a second barbed suture attached to the second bidimensional openworked knit, the sixth yarns cuts extending from said weft stitches of said at least one second weft stitched chain stitch forming said barbs of said second barbed suture.

In the present application, the terms “barbed suture”, “first barbed suture” and “second barbed suture” all relate to barbed sutures obtained according to the method of the invention and generally referred to as “barbed suture”, the terms “first barbed suture” and “second barbed suture” being used for sake of clarity when two needle-beds are used, as it may be useful to distinguish the first barbed sutures obtained with the first needle-bed from the second barbed sutures obtained with the second needle-bed.

As will appear from the description below, the method of the invention allows producing prosthetic meshes having barbed sutures attached thereto in a very simple, easy and rapid process. In particular the method of the invention is a cost effective process as there is no need to use sophisticated cutting machines with blades for performing cuts into the body of a monofilament.

It is known that warp knitting machines are capable of producing knits at high production rates. In addition, the knits produced may also show a very long dimension along the warp direction, which is the direction of manufacturing the knit.

As an example, with current existing warp knitting machines, knits of at least 300 meters long may be produced. For example, if the knitted structure of step a) of the method of the invention has a length L corresponding to the N stitches, a plurality of such knitted structures of length L may be obtained on a length of 300 meters, by simply repeating the knitting patterns of stitches 1 to N as many times as possible on the length of 300 meters. The method of the invention therefore allows manufacturing a plurality of meshes having barbed sutures attached thereto on 300 meters long in a very cost effective way, and in particular in only one knitting step.

The three-dimensional openworked knit obtained during step a)0) of the method of the invention is capable of favoring cellular growth and may be obtained thanks to all knitting patterns known from the art allowing to produce a knit with pores, voids, etc. on a double needle-bed warp machine by using the two needle-beds of the machine. Such knitting patterns are well known.

Examples of knitting three-dimensional knits suitable for the present invention are given in the documents WO99/05990, WO2009/031035 and WO2009/071998.

The bidimensional openworked knits obtained during step a)i) of the method of the invention are capable of favoring cellular growth and may be obtained thanks to all knitting patterns known from the art allowing to produce a knit with pores, voids, etc. using only one needle bed of a warp knitting machine. Such knitting patterns are well known.

Examples of knitting two-dimensional knits suitable for the present invention are given in the document WO2009/071998.

In addition, the barbs created in the barbed suture(s) of the mesh produced according to the method for the invention are ineradicable since they are made of yarns cuts, namely first yarns cuts and/or sixth yarns cuts, that stitch through chain stitches pillar.

In embodiments, the knitting pattern followed by the first guide bar B1 during step a)ii) produces at least a partial weft in which said first yarns complete weft stitches with a plurality of chain stitches, thereby producing a plurality of weft stitched chain stitches, and wherein the cutting of step b) is repeated for each weft stitched chain stitch, thereby producing a plurality of barbed sutures attached to the first knit portion.

In embodiments where the warp knitting machine comprises two needle-beds with three guide bars each as described above, the knitting pattern followed by the first guide bar B1 on the first needle-bed, respectively by the sixth guide bar B6 on the second needle-bed, during step a)ii), may produce at least a partial weft in which said first yarns, respectively said sixth yarns, complete weft stitches with a plurality of chain stitches, thereby producing a plurality of first and second weft stitched chain stitches. In such embodiments, the cutting of step b) may be repeated for each of said first and second weft stitched chain stitches, thereby producing a plurality of first barbed sutures attached to the first bidimensional openworked knit, respectively a plurality of second barbed sutures attached to the second bidimensional openworked knit.

The method of the invention therefore allows manufacturing a mesh having a plurality of barbed sutures of significant length each, the plurality of barbed sutures being attached to the mesh.

In current existing warp knitting machines, a high number of chain stitches may be produced along the width of a knit. As an example, 286 or more chain stitches may be produced on the width of a knit. The method of the invention therefore allows producing a mesh having for example from 2 to 20 barbed sutures attached thereto in one single knitting step

Guide bar B1, respectively guide bar B6, may be fed continuously or intermittently with the first yarns, respectively the sixth yarns, during step a)ii). In embodiments, guide bar B1, respectively guide bar B6, is fed continuously with the first yarns, respectively the sixth yarns, during step a)ii).

The method of the invention further allows producing meshes having barbed suture(s) having different functional portions along their length. In particular, the method of the invention allows producing meshes having barbed suture(s) having active portions, namely portions provided with barbs, and passive portions, namely portions free of any barbs. The passive portions may be obtained by simply stopping the feeding of the first guide bar B1, respectively the sixth guide bar B6, with the first yarns, respectively the sixth yarns, for a certain period of time during the knitting process of step ao) ii) of the method of the invention. Meshes with barbed sutures having alternating active portions and passive portions may therefore be obtained by simply intermittently feeding the first guide bar B1, respectively the sixth guide bar B6, during the knitting process. In embodiments, the first guide bar B1, alternatively the sixth guide bar B6, is fed intermittently with said first yarns, alternatively sixth yarns.

Alternatively, barbed sutures having alternating active portions and passive portions may be obtained by modifying the knitting pattern of guide bar B1, respectively of guide bar B6, so that, for one or several determined time periods during step a)ii) of production of the knitted structure, the first yarns, respectively the sixth yarns, do not complete any weft stitches with said weft stitched chain stitch(es).

The method of the invention further allows varying and selecting the length of the barbs according to an easy process. Indeed, the length of the barbs of the barbed sutures of the meshes obtained with the method of the invention will be dependent first on the distance left between a weft stitched chain stitch and the two adjacent chain stitches on both sides of said weft stitched chain stitch, said distance being a function of the knitting pattern used during step a)ii), and second on the location of the cutting line on said distance at the time of the cutting step b) of the method of the invention. The distance left between a weft stitched chain stitch and the two adjacent chain stitches in the first needle-bed second knit portion will be function of the threading-in of the three guide bars (B1, B2, B3) on the first needle-bed, in particular of the threading-in of the second and third guide bars B2 and B3, and optionally of the first guide bar B1. In the same manner, the distance left between a weft stitched chain stitch and the two adjacent chain stitches in the second needle-bed second knit portion will be function of the threading-in of the three guide bars (B4, B5, B6) on the second needle-bed, in particular of the threading-in of the fourth and fifth guide bars (B4, B5) forming the chain stitches. The greater the distance desired, the more empty needles left between two full needles. On the contrary, the smaller the distance desired between two adjacent weft stitched chain stitches, the less empty needles left between two full needles.

In embodiments where the warp knitting machine comprises only one needle-bed, the knitting pattern followed by the first guide bar B1, the second guide bar B2 and the third guide bar B3 may be as described below for a number N of stitches equal to 70, with x=30. All the knitting patterns are given according to the ISO 11676 standard (publication year 2014):

1o) during step a)i), production of the first knit portion capable of favoring cellular growth according to the following knitting pattern for stitches ranging from 1 to 30:

    • Bar B1: (5.4/3.2/0.1)×10//
    • Bar B2: (5.4/3.2/0.1)×10//
    • Bar B3: (0.1/2.3/5.4)×10//

2o) during step a)ii), production of the second knit portion according to the following knitting pattern for stitches ranging from 31 to 70:

    • Bar B1: (0.0/2.3/5.5/3.2)×10//
    • Bar B2: (2.3/2.3/3.2/3.2)×10//
    • Bar B3: (2.3/2.3/3.2/3.2)×10//

wherein, in both steps, B1 is threaded 1 full, 3 empty, B2 is threaded 1 full, 3 empty and B3 is threaded 1 full, 3 empty, along the whole width of the machine.

Such a pattern results in a distance between a weft stitched chain stitch and the two adjacent chain stitches of about 3.5 mm.

In embodiments, where the warp knitting machine comprises a first needle-bed comprising three guide bars B1, B2 and B3 and a second needle-bed comprising three guide bars B4, B5 and B6, the knitting patterns followed by the six guide bars may be as described below for a number N of stitches equal to 70, with x=30, and y=6. All the knitting patterns are given according to the ISO 11676 standard (publication year 2014):

1o) During step a)0): for stitches ranging from 1 to 6, production of a three-dimensional openworked knit capable of favoring cellular growth (connecting knit portion) according to the following knitting pattern:

    • B1: (5.4.3.3/3.2.1.1/0.1.3.3)×2//
    • B2: (5.4.3.3/3.2.1.1/0.1.3.3)×2//
    • B3: 0.1.0.1/2.3.2.3/5.4.2.2/0.1.2.2/2.3.4.4/5.4.2.2//
    • B4: 0.1.0.1/2.3.2.3/4.4.5.4/2.2.0.1/2.2.2.3/4.4.5.4//
    • B5: (3.3.5.4/3.3.3.2/1.1.0.1)×2//
    • B6: (3.3.5.4/3.3.3.2/1.1.0.1)×2//

2o) During step a)i): for stitches ranging from 7 to 30: production of the first knit portion as follows:

On the first needle-bed, production of a first bidimensional openworked knit capable of favoring cellular growth according to the following knitting pattern:

    • B1: (5.4.3.3/3.2.1.1/0.1.3.3)×8//
    • B2: (5.4.3.3/3.2.1.1/0.1.3.3)×8//
    • B3: (0.1.2.2/2.3.4.4/5.4.2.2)×8//

On the second needle-bed, production of a second bidimensional openworked knit capable of favoring cellular growth according to the following knitting pattern:

    • B4: (2.2.0.112.2.2.314.4.5.4)×8//
    • B5: (3.3.5.4/3.3.3.2/1.1.0.1)×8//
    • B6: (3.3.5.4/3.3.3.2/1.1.0.1)×8//

3o) During step a)ii): for stitches ranging from 31 à 70: production of the second knit portion as follows:

On the first needle-bed, production of first needle-bed second knit portion according to the following knitting pattern:

    • B1: (0.0.0.0/2.3.4.4/5.5.5.5/3.2.1.1)×10//
    • B2: (2.3.2.2/2.3.3.3/3.2.3.3/3.2.2.2)×10//
    • B3: (2.3.2.2/2.3.3.3/3.2.3.3/3.2.2.2)×10//

On the second needle-bed, production of second needle-bed second knit portion according to the following knitting pattern:

    • B4: (2.2.2.3/2.2.2.3/3.3.3.2/3.3.3.2)×10//
    • B5: (2.2.2.3/2.2.2.3/3.3.3.2/3.3.3.2)×10//
    • B6: (1.1.0.0/0.0.2.3/4.4.5.5/5.5.3.2)×10//

For example, in all the steps, all the guide bars (B1, B2, B3, B4, B5, B6) may be threaded 1 full, 3 empty along the whole width of the machine.

The method of the invention also allows varying and selecting the amount or number of barbs along the length of the suture in an easy way. In particular, the method of the invention allows selecting a specific frequency of barbs along the length of the suture, in other words a number of barbs per centimeter of suture. Such a frequency will depend on the knitting pattern followed by the first guide bar B1, respectively the sixth guide bar B6, threaded with the first yarns, respectively the sixth yarns. In particular, the more weft stitches completed along the warp direction of the chain stitch, the more weft stitches present on the weft stitched chain stitch in the end, and the higher the frequency of barbs on the resulting barbed suture. In embodiments, the knitting pattern followed by the first guide bar B1, respectively the sixth guide bar B6, produces a partial weft in which said first yarns, respectively said sixth yarns, complete from about 4 to about 15 weft stitches/cm along a length of each said weft stitched chain stitch.

In addition, the method of the invention allows producing meshes having barbed suture(s) attached thereto without affecting the tensile strength of the elongate body of the barbed suture(s). Indeed, contrary to cutting methods of the prior art which create the barbs by performing cuttings in the elongate body of the suture, made of a monofilament for example, the method of the invention leaves the yarn forming the elongate body of the suture integrate. The integrity of the yarn is not affected. As a consequence, the tensile strength of the yarn forming the elongate body of a barbed suture of the mesh obtained by the method of the invention is not affected by the presence of the barbs. Moreover, the method of the invention allows using both monofilaments and multifilaments yarns as the elongate body of the suture, whereas the methods of the prior art involving cutting steps request that the elongate body be a unitary structure, such as a monofilament yarn.

In embodiments, the chain stitch yarns, that will form the elongate body of the barbed suture(s), in particular the second, third, fourth and/or fifth yarns, may be monofilaments or multifilaments. In embodiments, the chain stitch yarns are monofilaments yarns, for example having a diameter ranging from about 0.07 mm to about 0.30 mm. In embodiments, the chain stitch yarns are multifilaments. Existing multifilament yarns may show high tenacity, in other words, high tensile strength. In embodiments, the chain stitch yarns may be multifilament yarns having a tensile strength ranging from about 25 cN/dTex to about 40 cN/dTex, for example a tensile strength of about 35 cN/dTex.

In embodiments, the chain stitch yarns may be multifilament yarns having a thickness ranging from 30 to 500 dTex, for example a thickness of 165 dTex.

In embodiments, the first yarns, that will form the barbs of the barbed suture, in particular of the first barbed suture when two needle-beds are used, may be monofilaments or multifilaments. In embodiments, the first yarns are monofilaments. In embodiments, the sixth yarns, that will form the barbs of the second barbed suture, may be monofilaments or multifilaments. In embodiments, the sixth yarns are monofilaments. Monofilaments allow obtaining barbs with higher mechanical properties. For example, the first yarns and the sixth yarns may be selected from monofilaments having a diameter ranging from about 0.15 mm to about 0.30 mm, for example from about 0.20 mm to about 0.30 mm.

The method of the invention allows producing meshes with barbed suture(s), with barbs having varying surface area in a very easy way. In particular, the size and/or the surface area of the barbs of a barbed suture of the mesh obtained by the method of the invention will be dependent on the size of the diameter of the first yarns, respectively the sixth yarns. In embodiments, the first yarns and/or the sixth yarns are monofilaments showing a diameter ranging from 0.07 mm to 0.30 mm. Such a diameter allows obtaining a good fixation of the barbed suture within the biological tissues.

Barbs of varying size may be desired depending on the contemplated surgical application of the mesh. For joining fat and relatively soft tissues, larger barbs may be desired, whereas smaller barbs may be more suitable for collagen-dense tissues. With the method of the invention, the production of small or alternatively large barbs may be easily obtained by simply selecting monofilament yarns for the first and/or sixth yarns of adequate diameters. For example, for obtaining a barbed suture with large barbs according to the method of the invention, monofilament yarns with a diameter ranging from 0.20 mm to 0.30 mm may be used for the first and/or sixth yarns. In embodiments, the first and/or sixth yarns are monofilament yarns showing a diameter ranging from 0.20 mm to 0.30 mm. Alternatively, for obtaining a barbed suture with small barbs according to the method of the invention, monofilament yarns with a diameter ranging from 0.07 mm to 0.10 mm may be used for the first and/or sixth yarns. In embodiments, the first and/or sixth yarns are monofilament yarns having a diameter ranging from 0.07 mm to 0.10 mm.

In some embodiments, a combination of large and small barbs within the same suture may be desirable, for example when the mesh of the invention is used in tissue repair with differing layer structures. Use of the combination of large and small barbs with the same suture wherein barb sizes are customized for each tissue layer will ensure maximum anchoring properties. In embodiments, the barbed suture(s) of the mesh obtained by the method of the invention may have both large and small barbs. Such barbed suture(s) with a combination of large and small barbs may be obtained by using monofilament yarns of a large diameter, for example ranging from 0.20 mm to 0.25 mm, for the first yarns which are threaded on the first guide bar B1, respectively for the sixth yarns which are threaded on the sixth guide bar B6, and monofilament yarns of a small diameter, for example ranging from 0.07 mm to 0.09 mm, for the second yarns which are threaded on the second guide bar B2, respectively for the fifth yarns which are threaded on the fifth guide bar B5, and monofilament yarns of a large diameter, for example ranging from 0.20 mm to 0.40 mm, for the third yarns which are threaded on the third guide bar B3, respectively for the fourth yarns which are threaded on the fourth guide bar B4.

All the yarns, namely the first, second, third, fourth, fifth and sixth yarns used for forming the knitted structure in the method of the invention are made of a biocompatible material. The biocompatible material may be identical or different from one yarn to another. The biocompatible material may be synthetic or natural. The biocompatible polymer material may be biodegradable, non-biodegradable or a combination of biodegradable and non-biodegradable. The term “biodegradable” as used herein is defined to include both bioabsorbable and bioresorbable materials. By biodegradable, it is meant that the materials decompose, or lose structural integrity under body conditions (e.g., enzymatic degradation or hydrolysis) or are broken down (physically or chemically) under physiologic conditions in the body such that the degradation products are excretable or absorbable by the body.

The biocompatible material may be selected from the group consisting of biodegradable polymers, non-biodegradable polymers, and combinations thereof.

Non-biodegradable materials that may be used as biocompatible material for the yarns of the method of the invention include polyolefins, such as polyethylene, polypropylene, copolymers of polyethylene and polypropylene, and blends of polyethylene and polypropylene; polyamides (such as nylon); polyamines, polyimines, polyesters such as polyethylene terephthalate; polytetrafluoroethylene; polyether-esters such as polybutester; polytetramethylene ether glycol; 1,4-butanediol; polyurethanes; and combinations thereof. In other embodiments, non-degradable materials may include silk, collagen, cotton, linen, carbon fibers, titanium, and the like. The polypropylene may be isotactic polypropylene or a mixture of isotactic and syndiotactic or atactic polypropylene.

Biodegradable materials that may be used as biocompatible material of the yarns of the method of the invention include polylactic acid (PLA), polyglycolic acid (PGA), oxidized cellulose, polycaprolactone (PCL), polydioxanone (PDO), trimethylene carbonate (TMC), polyvinyl alcohol (PVA), polyhydroxyalkanoates (PHAs), copolymers of these materials and mixtures thereof.

In embodiments, the biocompatible material is selected from polyethylene, polypropylene, polyester such as polyethylene terephthalates, polyamide, silicone, polyether ether ketone (PEEK), polyarylether ether ketone (PAEK), polylactic acid (PLA), polycaprolactone (PCL), polydioxanone (PDO), trimethylene carbonate (TMC), polyvinyl alcohol (PVA), polyhydroxyalkanoate (PHA), polyglycolic acid (PGA), copolymers of these materials, and mixtures thereof.

In embodiments, the biocompatible material used for the second and fifth yarns is polyethylene. The polyethylene may be a ultra high molecular weight polyethylene conferring to a multifilament yarn made therefrom a high tensile strength. In embodiments, the second and/or fifth yarns may be polyethylene multifilament yarns having a tensile strength ranging from about 25 cN/dTex to about 40 cN/dTex, for example a tensile strength of about 35 cN/dTex. Such polyethylene multifilament yarns made from ultra high molecular weight polyethylene and provided with such a tensile strength are commercially available from the company DSM under the tradename “Dyneema Purity®”.

In embodiments, the biocompatible material used for the second and fifth yarns is polyethylene terephthalate. In embodiments, the second and fifth yarns may be polyethylene terephthalate multifilament yarns having a tensile strength ranging from about 25 cN/dTex to about 40 cN/dTex, for example a tensile strength of about 35 cN/dTex. In other embodiments, the second and fifth yarns may be high tenacity polyester yarns having a thickness ranging from 30 to 500 dTex, for example of 165 dTex.

In embodiments, the biocompatible material used for the first, third, fourth and/or sixth yarns is polypropylene. In embodiments, the first, third, fourth and/or sixth yarns are polypropylene monofilaments. Polypropylene may confer rigidity to the monofilaments and therefore to the barbs obtained therefrom.

The method of the invention allows customizing the elongate body and the barbs of the barbed suture(s) attached to the mesh in function of the contemplated surgical application. For example, if the barbed suture(s) is/are to be used to fix the mesh in skin or tendon, the barbs may be made relatively short and more rigid, for example by using polypropylene monofilament for the first, third, fourth and/or sixth yarns, to facilitate entry into this rather firm tissue. Alternatively, if the barbed suture(s) is/are intended for use in fatty tissue, which is relatively soft, the barbs may be made longer and spaced further apart to increase the ability of the suture(s) to grip the soft tissue.

In a second step, step b), of the method of the invention, the second knit portion is cut along the warp direction on both sides of said at least one weft stitched chain stitch and along an edge separating the second knit portion from the first knit portion, so as to remove the second knit portion from the knitted structure while maintaining said weft stitched chain stitch attached to the first knit portion.

In embodiments, where the knitting pattern followed by the first guide bar B1 during step a)ii) produces at least a partial weft in which said first yarns complete weft stitches with a plurality of chain stitches, thereby producing a plurality of weft stitched chain stitches, the cutting of step b) is repeated for each weft stitched chain stitch, thereby producing a plurality of barbed sutures attached to the first knit portion.

In embodiments where the warp knitting machine comprises a first needle-bed comprising first, second and third guide bars (B1, B2, B3) and a second needle-bed comprising fourth, fifth and sixth guide bars (B4, B5, B6) as described above, the cutting step bo) may comprise the following steps:

cutting the first needle-bed second knit portion along the warp direction on both sides of said at least one first weft stitched chain stitch and along an edge separating the first needle-bed second knit portion from the first bidimensional openworked knit, so as to remove the first needle-bed second knit portion from the knitted structure while maintaining said at least one first weft stitched chain stitch attached to the first bidimensional openworked knit, the second or third yarn forming part of said at least one first weft stitched chain stitch forming the elongate body of a first barbed suture attached to the first bidimensional openworked knit, the first yarns cuts extending from said weft stitches of said at least one first weft stitched chain stitch forming said barbs of said first barbed suture,

cutting the second needle-bed second knit portion along the warp direction on both sides of said at least one second weft stitched chain stitch and along an edge separating the second needle-bed second knit portion from the second bidimensional openworked knit, so as to remove the second needle-bed second knit portion from the knitted structure while maintaining said at least one second weft stitched chain stitch attached to the second bidimensional openworked knit, the fourth or fifth yarn forming part of said at least one second weft stitched chain stitch forming the elongate body of a second barbed suture attached to the second bidimensional openworked knit, the sixth yarns cuts extending from said weft stitches of said at least one second weft stitched chain stitch forming said barbs of said second barbed suture.

In embodiments, said elongate body(ies) of said second barbed suture(s) is/are formed of fifth yarns only.

In embodiments, where the knitting pattern followed by the first guide bar B1 on the first needle-bed, respectively by the sixth guide bar B6 on the second needle-bed, during step a)ii), produces at least a partial weft in which said first yarns, respectively said sixth yarns, complete weft stitches with a plurality of chain stitches, thereby producing a plurality of first and second weft stitched chain stitches, the cutting of step b) is repeated for each of said first and second weft stitched chain stitches, thereby producing a plurality of first barbed sutures attached to the first bidimensional openworked knit, respectively a plurality of second barbed sutures attached to the second bidimensional openworked knit.

For each of such attached first and second weft stitched chain stitches, the chain stitch yarns, coming either from guide bar B2 (second yarns), B3 (third yarns), B4 (fourth yarns) and/or B5 (fifth yarns), preferably coming from guide bar B2 and/or guide bar B5, will form the elongate body of the thus obtained barbed sutures (first and/or second barbed sutures), and the first or sixth yarns cuts extending from the weft stitches of the first and second weft stitched chain stitches will form the barbs of the thus obtained barbed sutures (first and/or second barbed sutures).

In embodiments, the cutting step may be performed on line, namely while the knitted structure produced at step a) is still on the knitting machine. For example, the knitting machine may be provided with adequate blades. Alternatively, the cutting step may be performed off line, for example with pairs of scissors. For example, the cutting step may be performed by LASER cutting, high frequency welding cutting, roller cutting and/or hot resistance cutting.

In embodiments where the first and/or sixth yarns are monofilaments, the cutting step may be performed via melting the monofilaments at a temperature above their melting point so as to cut said monofilaments. Such a cutting step may be performed on line or off line.

In embodiments where the knitting machine used in the method of the invention comprises two needle-beds and six guide bars are used as described above, after the cutting step b) as described above, the knitted structure is then opened so as to spread in a single plane the part of the knitted structure obtained from the first needle-bed and the part of the knitted structure obtained from the second needle-bed,

wherein the first bidimensional openworked knit, the connecting knit portion, and the second bidimensional openworked knit form altogether the mesh; the second or third yarn forming part of said at least one first weft stitched chain stitch forms the elongate body of a first barbed suture attached to the first bidimensional openworked knit, the first yarns cuts extending from said weft stitches of said at least one first weft stitched chain stitch forming said barbs of said first barbed suture; the fourth or fifth yarn forming part of said at least one second weft stitched chain stitch forms the elongate body of a second barbed suture attached to the second bidimensional openworked knit, the sixth yarns cuts extending from said weft stitches of said at least one second weft stitched chain stitch forming said barbs of said second barbed suture.

In embodiments, for example when “y” is greater than 2, linking yarns from the three-dimensional openworked knit obtained in step a)0) may be cut along stitches ranging from 2 to y, such a step taking place after the cutting step b) described above and before opening the knitted structure in a single plane. The purpose of such a step is to reduce the height of the connecting knit portion in the final configuration of the mesh, when it is spread in a single plane, in order to avoid generating an extra thickness in the middle of the mesh.

After cutting step b) of the method of the invention, the first and/or sixth yarns cuts forming the barbs may generally extend substantially radially out of the chain stitch yarn forming the elongate body of the barbed suture along an angle between the first and/or sixth yarns cuts and the chain stitch yarn of about 90°. In the present application, the angle between the first and/or sixth yarns cuts and the yarn forming the elongate body is measured with a Profile Projector ORAM 300V geometric.

The angle between the first and/or sixth yarns cuts and the yarn forming the elongate body may be modified by submitting the attached barbed suture to a stretching treatment. For example, the angle between the first and/or sixth yarns cuts and the yarn forming the elongate body may be modified so that said angle reaches 45°, 35°, or 33°. The method of the invention therefore allows selecting the adequate angle between the barbs and the elongate body of the barbed suture for an optimized fixation in the biological tissues.

In embodiments, the method further comprises a stretching step during which the second knit portion produced in step a)ii) and/or the attached barbed suture(s) obtained in step bo) is(are) submitted to a stretching treatment. The stretching treatment may comprise a step of stretching the second knit portion or the attached barbed suture(s) in the warp direction. For example, the stretching treatment may be performed by using a traction testing machine such as Hounsfield model HSKS in which a first end of the second knit portion or the first end of an attached barbed suture is grasped by a fixed jaw of the machine and the opposite end of the second knit portion or of the attached barbed suture is grasped by a moving jaw. By moving away from the fixed jaw, the moving jaw stretches the second knit portion or the attached barbed suture.

On an industrial scale, the stretching treatment of the second knit portion in the warp direction may be performed on a heat-setting machine for example. By stretching the second knit portion in the warp direction, all weft stitched chain stitch(es) of the second knit portion are stretched, and as a consequence, all the attached barbed sutures are stretched.

In embodiments, the attached barbed suture(s) is/are stretched from about 0% to about 90%, which means that the stretched attached barbed suture(s) show(s) a length from about 0% to about 90% greater than the initial length of the attached barbed suture.

In embodiments, the second knit portion and/or the attached barbed suture(s) are stretched at 40%, which means that each of the second knit portion and/or the attached barbed suture(s) shows a length 40% greater than their initial length for each. Such a stretching step of 40% may result in the angle between the first and/or sixth yarns cuts and the yarn forming the elongate body be modified to reach about 45°. Such an angle between the first and/or sixth yarns cuts and the yarn forming the elongate body of the barbed suture may be desirable for barbed sutures intended to be used in soft biological tissues.

In other embodiments the second knit portion and/or the attached barbed suture(s) are stretched at 80%, which means that each of the second knit portion and/or the attached barbed suture(s) shows a length 80% greater than their initial length for each. Such a stretching step of 80% may result in the angle between the first and/or sixth yarns cuts and the yarn forming the elongate body be modified to reach about 35°. Such an angle between the first and/or sixth yarns cuts and the yarn forming the elongate body of the barbed suture may be desirable for barbed sutures intended to be used for anchoring purposes in dense biological tissues such as muscles.

In other embodiments the second knit portion and/or the attached barbed suture(s) are stretched at 90%, which means that each of the second knit portion and/or the attached barbed suture(s) shows a length 90% greater than their initial length for each. Such a stretching step of 90% may result in the angle between the first and/or sixth yarns cuts and the yarn forming the elongate body be modified to reach about 33°. Such an angle between the first and/or sixth yarns cuts and the yarn forming the elongate body of the barbed suture may be desirable for barbed sutures intended to be used for anchoring purposes in dense biological tissues such as muscles.

In embodiments, the attached barbed suture(s) may be submitted to a twisting treatment, for example for giving to the barbs a helical pattern. Such a treatment may be performed with a rotor machine.

In embodiments, the method of the invention further comprises a heat-setting step during which either the second knit portion produced in step a)ii) or the attached barbed suture(s) resulting from step b) is(are) submitted to a heat-setting treatment. The heat-setting treatment is intended to fix the barbed suture in the desired configuration. The heat-setting step may take place either between step a) and b), namely before the cutting step, or after step b), namely after the cutting step. For example, in case the second knit portion or the attached barbed suture(s) are submitted to a stretching treatment and/or a twisting treatment, they may simultaneously be submitted to a heat-setting treatment, so that the barbs configuration regarding for example the angle made between the first and/or sixth yarns cuts and the elongate body and/or the helical pattern obtained by the twisting treatment are fixed.

The heat-setting treatment may comprise a step of heating the second knit portion or the attached barbed suture(s) at a temperature ranging from 30° C. to 230° C. during a time period ranging from 1 min to 4 min. The heat-setting treatment may be performed on a heat-setting machine.

The mesh having one or more barbed suture(s) attached thereto obtained by the method of the invention may be sterilized by any means within the purview of those skilled in the art.

The barbed suture(s) of the mesh obtained by the method of the invention may be coated or impregnated with one or more medico-surgically useful substances which accelerate or beneficially modify the healing process when the barbed suture(s) is/are applied to a surgical site. In certain embodiments, the coating may be formed from biodegradable polymers selected from the group consisting of lactones, carbonates, polyorthoesters, hydroxyalkoanates, hydroxybutyrates, bioactive agents, polyanhydrides, silicone, calcium stearoyl lactylates, vinyl polymers, high molecular weight waxes and oils, natural polymers, proteins, polysaccharides, suspendable particulates, dispersible particulates, microspheres, nanospheres, rods, homopolymers thereof, copolymers thereof, and combinations thereof.

Suitable bioactive agents include, for example, biocidal agents, antimicrobial agents, antibiotics, anti-proliferatives, medicants, growth factors, anti-clotting agents, clotting agents, analgesics, anesthetics, anti-inflammatory agents, wound repair agents and the like, chemotherapeutics, biologics, protein therapeutics, monoclonal or polyclonal antibodies, DNA, RNA, peptides, polysaccharides, lectins, lipids, probiotics, diagnostic agents, angiogenics, anti-angiogenic drugs, polymeric drugs, and combinations thereof.

Bioactive agents include substances which are beneficial and tend to promote the healing process. For example, the barbed suture(s) of the mesh obtained by the method of the invention can be provided with a bioactive agent that will be deposited at the sutured site. The bioactive agent can be chosen for its antimicrobial properties, capability for promoting wound repair and/or tissue growth, or for specific indications such as thrombosis.

The barbed suture(s) of the mesh obtained by the method of the invention may additionally comprise a needle at their free end. The needle attachment may be made by any conventional method such as crimping, swaging, and the like.

The prosthetic mesh having one or more barbed suture(s) attached thereto obtained by the method of the invention may be utilized in any open endoscopic or laparoscopic methods. For example, the prosthetic mesh having one or more barbed suture(s) attached thereto obtained by the method of the invention may be utilized for the treatment of hernia.

For example, the mesh obtained by the method of the invention may play its function of abdominal wall repair while the one or more barbed sutures attached thereto may be used by the surgeon in order to fix the mesh to the abdominal wall. The surgeon does not have to look for sutures at the time he needs to fix the mesh to the biological tissue. Moreover, because of the barbed nature of the suture(s) attached to the mesh, the surgeon needs not perform surgical knots. The barbs of the attached barbed suture(s) perform the anchoring function of the suture into the biological tissue very efficiently.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING

The advantages of the method of the invention will appear more clearly from the following examples and attached drawings in which:

FIG. 1 is a schematic top view showing an embodiment of the knitted structure obtained in step a) of the method of the invention in the case where one needle-bed is used,

FIG. 2 is a schematic view showing an embodiment of a knitting pattern suitable for the knitting process of step ao) ii) of the method of the invention in the case where one needle-bed is used such as in FIG. 1,

FIG. 3 is a schematic view showing the cutting step of the method of the invention for the knitted structure of FIG. 1,

FIG. 4 is a schematic top view showing a mesh having a barbed suture attached thereto obtained after performing step bo) of the method of the invention on the knitted structure of FIG. 1,

FIG. 5 is a partial front view of an attached barbed suture obtained by the method of the invention showing the angle formed between the barbs and the elongate body of the suture,

FIG. 6 is a partial schematic view of an attached barbed suture obtained after step bo) of the method of the invention having active and passive portions along its length,

FIG. 7 is a schematic side view showing the knitted structure obtained in step a) of the method of the invention in the case where two needle-beds are used,

FIG. 8 is a schematic top view of the knitted structure of FIG. 7,

FIG. 9 is a schematic top view of the knitted structure of FIG. 7 after cutting step bo),

FIG. 10 is a schematic side view showing optional step co),

FIG. 11 is a side view of the prosthetic mesh of the invention obtained from the knitted structure of FIG. 7 after step do),

FIG. 12 is a top view of the prosthetic mesh of the invention obtained from the knitted structure of FIG. 7 after step do).

DETAILED DESCRIPTION OF THE INVENTION Examples Example 1

In the present example, a prosthetic mesh 1 (see FIG. 4) having an attached barbed suture 10 attached thereto is formed according to the method of the invention, using on needle-bed only.

In a first step, step ao), a knitted structure 2 (see FIG. 1) is produced on a Raschel machine comprising one needle-bed comprising a first guide bar B1, a second guide bar B2 and a third guide bar B3. The knitted structure is produced on a determined length along the warp direction corresponding to a total number N of 70 stitches, with x=30.

In other embodiments, the knitted structure could be produced on other lengths corresponding to other number of stitches.

In the present example, all the knitting patterns are given according to the ISO 11676 standard (publication year 2014).

With reference to FIG. 1, is shown schematically a piece of the knitted structure 2, with the first knit portion 13 and the second knit portion 12, and the edge 14 separating the first knit portion 13 from the second knit portion 12. The knitted structure 2 is produced as described below.

In a step a)i), the first knit portion 13 capable of favoring cellular growth is produced for stitches ranging from 1 to 30.

The knitting pattern followed by bars B1, B2 and B3 is the following one:

    • Bar B1: (5.4/3.2/0.1)×10//
    • Bar B2: (5.4/3.2/0.1)×10//
    • Bar B3: (0.1/2.3/5.4)×10//

In a step a)ii), the second knit portion 12 is produced for stitches ranging from 31 to 70.

The knitting pattern followed by bars B1, B2 and B3 is the following one:

    • Bar B1: (0.0/2.3/5.5/3.2)×10//
    • Bar B2: (2.3/2.3/3.2/3.2)×10//
    • Bar B3: (2.3/2.3/3.2/3.2)×10//

In both steps a)i) and aii), B1 is threaded 1 full, 3 empty, B2 is threaded 1 full, 3 empty and B3 is threaded 1 full, 3 empty, along the whole width of the machine.

Such a pattern results in a distance between a weft stitched chain stitch and the two adjacent chain stitches of about 3.5 mm.

The yarns threaded in guide bar B1 (first yarns) are polypropylene monofilaments having a diameter of 0.20 mm.

The yarns threaded in guide bar B2 (second yarns) are multifilament yarns of ultra high molecular weight polyethylene, such as those marketed by the company DSM under the tradename “Dyneema Purity®”. These multifilaments have a tensile strength of 35 cN/dTex.

The yarns threaded in guide bar B3 (third yarns) are polypropylene monofilaments having a diameter of 0.30 mm.

With reference to FIG. 2 showing the knitting pattern of step a)ii) above in accordance with a representation well known for one skilled in the art, are shown the warp direction Wa, the weft direction We, the first yarns “a” (threaded in guide bar B1) shown as a thick line, the second yarns “b” (threaded in guide bar B2) shown as a dotted line, and the third yarns “c” (threaded in guide bar B3) shown as a thin line. The knitting pattern produces a plurality of chain stitches 3 (with second and third yarns (b, c) coming from guide bars B2 and B3) and a partial weft 4 (with first yarns “a” coming from guide bar B1). The first yarns “a” complete weft stitches 5 with some of the chain stitches 3, herein after called weft stitched chain stitches 6. Actually, as appears from FIG. 2, the knitting pattern produces one weft stitched chain stitch 6 out of two chain stitches 3 present in the second knit portion 12. In the present example, it happens that the weft stitched chain stitches 6 correspond to all the chain stitches 3 that are made with the second yarns “b”. In other embodiments not shown, the weft stitched chain stitches 6 could correspond to the chain stitches 3 that are made with the third yarns “c”, or could correspond to some of the chain stitches made with the second yarns “b” or with the third yarns “c”. In the present example, the distance between two adjacent weft stitched chain stitches 6 is due to the threading-in of the second guide bar B2, which is 1 full, 3 empty. Such a threading-in may result in a distance between the weft stitched chain stitches 6 of about 3.5 cm.

With reference to FIG. 3, in a second step, step bo), the second knit portion 12 thus produced is cut along the warp direction on both sides of the weft stitched chain stitches 6 and along the edge 14 separating the second knit portion 12 from the first knit portion 13 along cutting lines 11, so as to remove the second knit portion 12 from the knitted structure 2 while maintaining the weft stitched chain stitch 6 attached to the first knit portion 13. The cutting step may be performed for example with a pair of scissors.

For sake of clarity, the figures show the cutting step for one weft stitched chain stitch 6 only. Anyway, the cutting step may be repeated for each weft stitched chain stitch 6 present on the width of the knitted structure 2 corresponding to the desired width of the final mesh 1 to be obtained.

FIG. 4 shows the mesh 1 having an attached barbed suture 10 obtained in the present example with the method of the invention, with the first knit portion 13 forming the mesh and the attached weft stitched chain stitch 6, in which the chain stitch yarn (second yarn “b” with reference to FIG. 2) of the weft stitched chain stitch 6 forms the elongate body 9 of the barbed suture 10 and the monofilament cuts 7 coming from first yarns “a” and extending from the weft stitches 5 of the weft stitched chain stitch 6 form the barbs 8 of the barbed suture 10.

As shown on this Figure, the attached weft stitched chain stitch 6 which is also the elongate body 9 of the attached barbed suture 10 extends along a longitudinal axis A1, and the monofilament cuts 7, which are also the barbs 8, each extend along a longitudinal axis A2. On

FIG. 4, the angle α between axis A1 and axis A2 is substantially about 90°.

As appears from the cutting step shown on FIG. 3, the length of the monofilament cuts 7, and therefore of the barbs 8, depend both on the initial distance between the weft stitched chain stitch 6 and adjacent chain stitches 3, and on the location of the cutting lines 11.

Although FIG. 4 shows the mesh 1 with only one attached barbed suture 10, a plurality of attached barbed sutures 10 could be obtained depending on the number of weft stitched chain stitches 6 cut along the width of the knitted structure 2 corresponding to the desired width of the final mesh 1 to be obtained.

With reference to FIG. 6 is shown schematically a portion of an attached barbed suture 10 obtained according to the method of the present example in the case where the first guide bar B1 was fed intermittently with the first yarns. During the time periods for which the guide bar B1 was not fed with the first yarns, no weft stitches were produced on the weft stitched chain stitch 6, thereby resulting in portions of the weft stitched chain stitch 6 free of barbs, namely passive portions 15. An attached barbed suture 10 having alternating active portions 16 (when guide bar B1 was fed with first yarns) and passive portions 15 is therefore obtained. As shown on this Figure, the respective distances (L1, L2) between two adjacent active portions 16 may vary, as such distances are dependent on the time period during which the guide bar B1 was not fed.

With reference to FIG. 5 is shown a larger view of a portion of the attached barbed suture 10 of FIG. 4 after a stretching treatment in which the attached barbed suture was stretched at 90%. As appears from this Figure, after the stretching treatment, the angle α between axis A1 and axis A2, in other words between the yarn “b” forming the elongate body 9 of the barbed suture 10 and the monofilament cuts 7, also barbs 8, has been modified and is now about 33°.

The attached barbed suture 10 of FIG. 5 is then submitted to a heat-setting treatment in order to fix the configuration of the barbs 8 with respect to the elongate body 9 of the suture 10.

In embodiments not shown, the knitting pattern used in step a)ii) above may result in all chain stitches being also weft stitched chain stitches, when the first yarns produce weft stitches with all chain stitches produced by the second and the third guide bars. In other embodiments, the knitting pattern may produce only one weft stitched chain stitch out of three, four, five, etc. . . . chain stitches present in the second knit portion, which may result in variations of the distance between two adjacent weft stitched chain stitches. Alternatively, this distance may vary due to different threading-in of the guide bars.

The mesh 1 with the barbed suture 10 attached thereto may be particularly useful in hernia repair. The mesh may play its function of abdominal wall repair while the one or more barbed sutures 10 attached thereto may be used by the surgeon in order to fix the mesh to the abdominal wall. The surgeon does not have to look for sutures at the time he needs to fix the mesh to the biological tissue. Moreover, because of the barbed nature of the suture(s) attached to the mesh, the surgeon needs not perform surgical knots. The barbs of the attached barbed suture(s) perform the anchoring function of the suture into the biological tissue very efficiently.

Example 2

In the present example, a prosthetic mesh 28 having a plurality of barbed sutures (10; 10′) attached thereto (see FIG. 12) is formed according to the method of the invention using two needle-beds. The knitting machine used may be a Raschel knitting machine comprising a double needle-bed. The description of the method used in the present example is made with reference to FIGS. 7-12.

The Raschel knitting machine comprises a first needle-bed comprising three guide bars B1, B2 and B3 and a second needle-bed comprising three guide bars B4, B5 and B6. In the present example, the same references that are used for the production and steps performed in relation to the first needle-bed will be maintained for the production and steps performed in relation to the first needle-bed, but with a “prime” indicated after the reference digit.

In the present example, all the guide bars (B1, B2, B3, B4, B5, B6) are threaded 1 full, 3 empty along the whole width of the machine and all the knitting patterns are given according to the ISO 11676 standard (publication year 2014).

In the present example:

first guide bar B1 is threaded with first yarns and sixth guide bar B6 is threaded with sixth yarns, the first and sixth yarns being monofilaments of polypropylene having a diameter of about 0.20 mm,

second guide bar B2 is threaded with second yarns, and fifth guide bar B5 is threaded with fifth yarns, the second and fifth yarns being multifilaments of high tenacity polyester having a thickness of 165 dTex,

third guide bar B3 is threaded with third yarns and fourth guide bar B4 is threaded with fourth yarns, the third and fourth yarns being monofilaments of polypropylene having a diameter of about 0.30 mm.

In a first step a), a knitted structure 27 (see FIG. 7) is produced on a length in the warp direction Wa corresponding to a number N of 70 stitches, with x=30 and y=6. The warp direction Wa is indicated on FIG. 7. Although this warp direction is not repeated for FIGS. 8-10 for sake of clarity, it is identical for these Figures as in FIG. 7.

1o) During step a)0): for stitches ranging from 1 to 6, a connecting portion 20 is produced under the form of a three-dimensional openworked knit 21 capable of favoring cellular growth, according to the following knitting pattern:

    • B1: (5.4.3.3/3.2.1.1/0.1.3.3)×2//
    • B2: (5.4.3.3/3.2.1.1/0.1.3.3)×2//
    • B3: 0.1.0.1/2.3.2.3/5.4.2.2/0.1.2.2/2.3.4.4/5.4.2.2//
    • B4: 0.1.0.1/2.3.2.3/4.4.5.4/2.2.0.1/2.2.2.3/4.4.5.4//
    • B5: (3.3.5.4/3.3.3.2/1.1.0.1)×2//
    • B6: (3.3.5.4/3.3.3.2/1.1.0.1)×2//

The above knitting pattern allows producing a knit that has a first face produced on the first needle-bed by the first, second and third yarns from the first, second and third guide bars (B1, B2, B3), and a second face, produced on the second needle-bed by the fourth, fifth and sixth yarns from the fourth, fifth and sixth guide bars (B4, B5, B6), the first and second faces being linked together by some of the third and/or fourth, yarns crossing from the first needle-bed to the second needle-bed and vice-versa, thereby forming linking yarns.)

2o) During step a)i): for stitches ranging from 7 to 30: a first knit portion 22 is produced. During this step and the subsequent step, independent knits are produced on each of the needle bed in parallel.

On the first needle-bed, a first bidimensional openworked knit 23 capable of favoring cellular growth is produced according to the following knitting pattern:

B1: (5.4.3.3/3.2.1.1/0.1.3.3)×8//

    • B2: (5.4.3.3/3.2.1.1/0.1.3.3)×8//
    • B3: (0.1.2.2/2.3.4.4/5.4.2.2)×8//

On the second needle-bed, a second bidimensional openworked knit 23′ capable of favoring cellular growth is produced according to the following knitting pattern:

    • B4: (2.2.0.1/2.2.2.3/4.4.5.4)×8//
    • B5: (3.3.5.4/3.3.3.2/1.1.0.1)×8//
    • B6: (3.3.5.4/3.3.3.2/1.1.0.1)×8//

The first and second bidimensional openworked knits being independent from each other. They each constitute a bidimensional knit suitable for use as a reinforcement member for the repair of hernia in the abdominal wall.

3o) During step a)ii): for stitches ranging from 31 to 70: a second knit portion 24 is produced.

On the first needle-bed, a first needle-bed second knit portion 25 is produced according to the following knitting pattern:

    • B1: (0.0.0.0/2.3.4.4/5.5.5.5/3.2.1.1)×10//
    • B2: (2.3.2.2/2.3.3.3/3.2.3.3/3.2.2.2)×10//
    • B3: (2.3.2.2/2.3.3.3/3.2.3.3/3.2.2.2)×10//

In a similar way as described in Example 1 for the second knit portion 12, in the present example, the knitting pattern followed by the second and third guide bars (B2, B3) produces chain stitches and the knitting pattern followed by the first guide bar B1 produces a partial weft in which said first yarns complete weft stitches with a plurality, four in the example shown in the Figures, of said chain stitches, thereby producing a plurality of weft stitched chain stitches 6, four in the example shown.

On the second needle-bed, a second needle-bed second knit portion 25′ is produced according to the following knitting pattern:

    • B4: (2.2.2.3/2.2.2.3/3.3.3.2/3.3.3.2)×10//
    • B5: (2.2.2.3/2.2.2.3/3.3.3.2/3.3.3.2)×10//
    • B6: 1.1.0.0/0.0.2.3/4.4.5.5/5.5.3.2)×10//

Similarly to what takes place for the first-needle bed, the knitting pattern followed by the fourth and fifth guide bars (B4, B5) produces chain stitches and the knitting pattern followed by the sixth guide bar B6 produces a partial weft in which the sixth yarns complete weft stitches with a plurality, four as shown on the Figures, of said chain stitches, thereby producing a plurality of weft stitched chain stitches, for example four weft stitched chain stitches 6′.

The knitted structure 27 produced in the step a) above is shown on FIGS. 7 and 8 which are schematic side view and bottom view of the knitted structure.

In a step bo), with reference to FIGS. 9-12:

the first needle-bed second knit portion 25 is cut along the warp direction on both sides of each of the four weft stitched chain stitches 6 obtained by first, second and third guide bars (B1, B2, B3) and along an edge 26 separating the first needle-bed second knit portion 25 from the first bidimensional openworked knit 23, so as to remove the first needle-bed second knit portion 25 from the knitted structure 27 while maintaining the four weft stitched chain stitches 6 attached to the first bidimensional openworked knit 23,

the second needle-bed second knit portion 25′ is cut along the warp direction on both sides of each of the four weft stitched chain stitches 6′ obtained by third, fourth and fifth guide bars (B4, B5, B6) and along an edge 26′ separating the second needle-bed second knit portion 25′ from the second bidimensional openworked knit 23′, so as to remove the second needle-bed second knit portion 25′ from the knitted structure 27 while maintaining the four weft stitched chain stitches 6′ attached to the second bidimensional openworked knit 23′.

The cutting step is performed in the same manner as described in Example 1.

In a step co), with reference to FIG. 10, the linking yarns from the three-dimensional openworked knit 21 obtained in step a)0) are cut along stitches ranging from 2 to 6. As a result, the connecting knit portion 20 comprises a cut part 20a and a bridge part 20b, said bridge part 20b connecting the part of the knitted structure 27 obtained on the first needle-bed to the part of the knitted structure 27 obtained on the second needle-bed.

This step may be optional, for example in the case where the connecting knit portion 20 extends already on a length corresponding to 2 stitches only from the start. The purpose of this step co) is to reduce the height of the connecting knit portion in the final configuration of the mesh as shown in FIG. 11, in order to avoid generating an extra thickness in the middle of the mesh 28.

If the number of stitches in the warp direction along which the connecting knit portion extends from the start is low enough for not producing any extra thickness in the final configuration of the mesh, than the present step co) is unnecessary.

In a step do), the knitted structure 27 is opened so as to spread in a single plane the part of the knitted structure obtained from the first needle-bed and the part of the knitted structure obtained from the second needle-bed as shown on FIGS. 11 and 12.

With reference to FIGS. 11 and 12, the first bidimensional openworked knit 23, the connecting knit portion 20, cut according to step co), and the second bidimensional openworked knit 23′ form altogether the mesh 28: this mesh 28 is made of knits capable of favoring cellular growth and is therefore particularly indicated for repair of the abdominal wall for example. The second yarns forming part of the weft stitched chain stitches 6 obtained by first, second and third guide bars (B1, B2, B3) form the elongate body 9 of first barbed sutures 10 attached to the first bidimensional openworked knit 23, the monofilament cuts 7 of first yarns extending from the weft stitches of the weft stitched chain stitches 6 form the barbs 8 of the first barbed sutures 10; the fifth yarns forming part of the weft stitched chain stitches 6′ obtained by fourth, fifth and sixth guide bars (B4, B5, B6) form the elongate body 9′ of second barbed sutures 10′ attached to the second bidimensional openworked knit 23′, the monofilament cuts 7′ of sixth yarns extending from the weft stitches of the weft stitched chain stitches 6′ form the barbs 8′ of the second barbed sutures 10′.

In the present example, the elongate bodies 9 of the first barbed sutures 10 are formed of second yarns only and the elongate bodies 9′ of the second barbed sutures 10′ are formed of fifth yarns only.

In other embodiments not shown, the elongate bodies 9 of the first barbed sutures 10 may be formed of third yarns only or of a combination of second and third yarns, and the elongate bodies 9′ of the second barbed sutures 10′ may be formed of fourth yarns only or of a combination of fourth and fifth yarns.

The mesh 28 having barbed sutures (10, 10′) attached thereto as obtained in the present example may be particularly useful in hernia repair. The mesh 28 may play its function of abdominal wall repair while the barbed sutures (10, 10′) attached thereto may be used by the surgeon in order to fix the mesh 28 to the abdominal wall. The surgeon does not have to look for sutures at the time he needs to fix the mesh to the biological tissue. Moreover, because of the barbed nature of the suture(s) (10, 10′) attached to the mesh 28, the surgeon needs not perform surgical knots. As appears from FIGS. 11 and 12, the barbs (8, 8′) of the attached barbed suture(s) (10, 10′) are naturally oriented in opposite direction, thereby performing efficiently their anchoring function of the suture (10; 10′) and of the mesh 28 into the biological tissue.

In addition, the attached barbed sutures (10; 10′) of the mesh 28 may be further submitted to a treatment, such as a stretching treatment, a twisting treatment, a heat-setting treatment and/or a combination of these treatments, so as to provide them with an optimized configuration in function of the intended use of the mesh and sutures, in order to ensure an optimized fixation of the mesh in the biological tissues.

The method of the invention allows preparing prosthetic meshes having one or more barbed suture(s) attached thereto in a very simple way, and in only one single knitting process. The method further allows adapting very easily and in a cost effective manner the nature and structure of the attached barbed suture(s), such as frequency per cm, configuration, spacing, length and surface area of the barbs, depending upon the tissue in which the barbed suture(s) are to be used. With the method of the invention, it is possible to obtain meshes having barbed suture(s) attached thereto, with barbed suture(s) in which the barbs may be arranged in any suitable pattern, for example, helical, linear, or randomly spaced.

Claims

1. A prosthesis for hernia repair comprising

a mesh including a first knit portion including at least first and second biocompatible yarns, and
at least one barbed suture attached to the first knit portion, the barbed suture including an elongate body and a plurality of first yarn cuts extending substantially radially out from the elongate body forming barbs, the elongate body having at least one weft stitched chain stitch made from at least one of the second biocompatible yarn or a third biocompatible yarn, and the first yarn cuts made from the first biocompatible yarns stitched to the at least one second or third biocompatible yarns of the elongate body.

2. The prosthesis of claim 1, wherein the first yarn cuts forming the barbs extend from the weft stitch of the at least one weft stitched chain stitch of the elongate body.

3. The prosthesis of claim 1, wherein the elongate body includes a plurality of weft stitched chain stitches.

4. The prosthesis of claim 1, wherein the at least one weft stitched chain stitch is made from both the second and third biocompatible yarns.

5. The prosthesis of claim 1, wherein the first biocompatible yarn forms the weft stitch of the weft stitched chain stitch, and the second and third biocompatible yarns form the chain stitch of the weft stitched chain stitch.

6. The prosthesis of claim 1, wherein the elongate body of the barbed suture is formed of the second biocompatible yarns only.

7. The prosthesis of claim 1, wherein the first knit portion further includes the third biocompatible yarn.

8. The prosthesis of claim 1, wherein the mesh and the barbed suture are a knitted structure having a determined length in a warp direction corresponding to a total number of N stitches ranging from 1 to N in the warp direction, N being an integer above 7, wherein the total number of N stitches includes a number of stitches for the first knit portion ranging from 1 to x, where 1<x<N and a number of stitches for the elongate body ranging from (x+1) to N.

9. The prosthesis of claim 1, wherein the at least one barbed suture has a final length from about 0% to about 90% greater than an initial knit length of the at least one barbed suture.

10. The prosthesis of claim 1, wherein the at least one barbed suture has a final length of about 40% greater than an initial knit length of the at least one barbed suture.

11. The prosthesis of claim 1, wherein the at least one barbed suture has a final length about 40% greater than an initial knit length of the at least one barbed suture and includes an angle of about 45° between the first yarn cuts and the elongate body.

12. The prosthesis of claim 1, wherein the at least one barbed suture includes one or more medico-surgically useful substances.

13. The prosthesis of claim 1, wherein the at least one barbed suture additionally includes a needle on a free end of the elongate body.

14. The prosthesis of claim 1, wherein the first knit portion includes at least one weft stitched chain stitch.

15. The prosthesis of claim 1, wherein the at least one barbed suture includes active portions including the barbs and passive portions free of the barbs with varying lengths therebetween along the elongate body.

16. The prosthesis of claim 1, wherein the at least one barbed suture is stretched, twisted, heat-set, or combinations thereof.

17. The prosthesis of claim 1, wherein the first knit portion is an openworked knit capable to favoring cellular growth.

Referenced Cited
U.S. Patent Documents
1187158 June 1916 Mcginley
3054406 September 1962 Usher
3118294 January 1964 Laethem
3124136 March 1964 Usher
3272204 September 1966 Artandi et al.
3276448 October 1966 Kronenthal
3320649 May 1967 Naimer
3364200 January 1968 Ashton et al.
3570482 March 1971 Shigeru et al.
3718725 February 1973 Hamano
4006747 February 8, 1977 Kronenthal et al.
4060081 November 29, 1977 Yannas et al.
4173131 November 6, 1979 Melton et al.
4193137 March 18, 1980 Heck
4248064 February 3, 1981 Odham
4294241 October 13, 1981 Miyata
4307496 December 29, 1981 Nakagaki et al.
4307717 December 29, 1981 Hymes et al.
4338800 July 13, 1982 Matsuda
4476697 October 16, 1984 Schafer et al.
4487865 December 11, 1984 Balazs et al.
4500676 February 19, 1985 Balazs et al.
4511653 April 16, 1985 Play et al.
4527404 July 9, 1985 Nakagaki et al.
4591501 May 27, 1986 Cioca
4597762 July 1, 1986 Walter et al.
4603695 August 5, 1986 Ikada et al.
4631932 December 30, 1986 Sommers
4670014 June 2, 1987 Huc et al.
4709562 December 1, 1987 Matsuda
4748078 May 31, 1988 Doi et al.
4759354 July 26, 1988 Quarfoot
4769038 September 6, 1988 Bendavid et al.
4796603 January 10, 1989 Dahlke et al.
4813942 March 21, 1989 Alvarez
4841962 June 27, 1989 Berg et al.
4854316 August 8, 1989 Davis
4925294 May 15, 1990 Geshwind et al.
4931546 June 5, 1990 Tardy et al.
4942875 July 24, 1990 Hlavacek et al.
4948540 August 14, 1990 Nigam
4950483 August 21, 1990 Ksander et al.
4970298 November 13, 1990 Silver et al.
4976737 December 11, 1990 Leake
5002551 March 26, 1991 Linsky et al.
5015584 May 14, 1991 Brysk
5116357 May 26, 1992 Eberbach
5147374 September 15, 1992 Fernandez
5162430 November 10, 1992 Rhee et al.
5171273 December 15, 1992 Silver et al.
5176692 January 5, 1993 Wilk et al.
5192301 March 9, 1993 Kamiya et al.
5195542 March 23, 1993 Gazielly et al.
5196185 March 23, 1993 Silver et al.
5201745 April 13, 1993 Tayot et al.
5201764 April 13, 1993 Kelman et al.
5206028 April 27, 1993 Li
5217493 June 8, 1993 Raad et al.
5254133 October 19, 1993 Seid
5256418 October 26, 1993 Kemp et al.
5258000 November 2, 1993 Gianturco
5263983 November 23, 1993 Yoshizato et al.
5304595 April 19, 1994 Rhee et al.
5306500 April 26, 1994 Rhee et al.
5324775 June 28, 1994 Rhee et al.
5328955 July 12, 1994 Rhee et al.
5334527 August 2, 1994 Brysk
5339657 August 23, 1994 Mcmurray
5350583 September 27, 1994 Yoshizato et al.
5356432 October 18, 1994 Rutkow et al.
5368549 November 29, 1994 Mcvicker
5368602 November 29, 1994 Torre
5370650 December 6, 1994 Jonathan et al.
5376375 December 27, 1994 Rhee et al.
5376376 December 27, 1994 Li
5397331 March 14, 1995 Himpens et al.
5399361 March 21, 1995 Song et al.
5413791 May 9, 1995 Rhee et al.
5425740 June 20, 1995 Hutchinson, Jr.
5428022 June 27, 1995 Palefsky et al.
5433996 July 18, 1995 Kranzler et al.
5441491 August 15, 1995 Verschoor et al.
5441508 August 15, 1995 Gazielly et al.
5456693 October 10, 1995 Conston et al.
5456711 October 10, 1995 Hudson
5466462 November 14, 1995 Rosenthal et al.
5480644 January 2, 1996 Freed
5487895 January 30, 1996 Dapper et al.
5490984 February 13, 1996 Freed
5512291 April 30, 1996 Li
5512301 April 30, 1996 Song et al.
5514181 May 7, 1996 Light et al.
5522840 June 4, 1996 Krajicek
5523348 June 4, 1996 Rhee et al.
5536656 July 16, 1996 Kemp et al.
5543441 August 6, 1996 Rhee et al.
5565210 October 15, 1996 Rosenthal et al.
5567806 October 22, 1996 Abdul-Malak et al.
5569273 October 29, 1996 Titone et al.
RE35399 December 10, 1996 Eisenberg
5593441 January 14, 1997 Lichtenstein et al.
5595621 January 21, 1997 Light et al.
5601571 February 11, 1997 Moss
5607474 March 4, 1997 Athanasiou et al.
5607590 March 4, 1997 Shimizu
5614587 March 25, 1997 Rhee et al.
5618551 April 8, 1997 Tardy et al.
5634931 June 3, 1997 Kugel
5639796 June 17, 1997 Lee
5665391 September 9, 1997 Lea
5667839 September 16, 1997 Berg
5676967 October 14, 1997 Williams et al.
5681568 October 28, 1997 Goldin et al.
5686090 November 11, 1997 Schilder et al.
5686115 November 11, 1997 Vournakis et al.
5690675 November 25, 1997 Sawyer et al.
5695525 December 9, 1997 Mulhauser et al.
5697978 December 16, 1997 Sgro
5700476 December 23, 1997 Rosenthal et al.
5700477 December 23, 1997 Rosenthal et al.
5702416 December 30, 1997 Kieturakis et al.
5709934 January 20, 1998 Bell et al.
5711960 January 27, 1998 Shikinami
5716409 February 10, 1998 Debbas
5720981 February 24, 1998 Eisinger
5732572 March 31, 1998 Litton
5743917 April 28, 1998 Saxon
5749895 May 12, 1998 Sawyer et al.
5752974 May 19, 1998 Rhee et al.
5766246 June 16, 1998 Mulhauser et al.
5766631 June 16, 1998 Arnold
5769864 June 23, 1998 Kugel
5771716 June 30, 1998 Schlussel
5785983 July 28, 1998 Furlan et al.
5800541 September 1, 1998 Rhee et al.
5814328 September 29, 1998 Gunasekaran
5833705 November 10, 1998 Ken et al.
5840011 November 24, 1998 Landgrebe et al.
5861034 January 19, 1999 Taira et al.
5863984 January 26, 1999 Doillon et al.
5869080 February 9, 1999 Mcgregor et al.
5871767 February 16, 1999 Dionne et al.
5876444 March 2, 1999 Lai
5891558 April 6, 1999 Bell et al.
5899909 May 4, 1999 Claren et al.
5906937 May 25, 1999 Sugiyama et al.
5910149 June 8, 1999 Kuzmak
5911731 June 15, 1999 Pham et al.
5916225 June 29, 1999 Kugel
5919232 July 6, 1999 Chaffringeon et al.
5919233 July 6, 1999 Knopf et al.
5922026 July 13, 1999 Chin
5931165 August 3, 1999 Reich et al.
5942278 August 24, 1999 Hagedorn et al.
5962136 October 5, 1999 Dewez et al.
5972022 October 26, 1999 Huxel
RE36370 November 2, 1999 Li
5993844 November 30, 1999 Abraham et al.
5994325 November 30, 1999 Roufa et al.
5997895 December 7, 1999 Narotam et al.
6001895 December 14, 1999 Harvey et al.
6008292 December 28, 1999 Lee et al.
6015844 January 18, 2000 Harvey et al.
6039686 March 21, 2000 Robert
6042534 March 28, 2000 Gellman et al.
6042592 March 28, 2000 Schmitt
6043089 March 28, 2000 Sugiyama et al.
6051425 April 18, 2000 Morota et al.
6056688 May 2, 2000 Benderev et al.
6056970 May 2, 2000 Greenawalt et al.
6057148 May 2, 2000 Sugiyama et al.
6063396 May 16, 2000 Kelleher
6066776 May 23, 2000 Goodwin et al.
6066777 May 23, 2000 Benchetrit
6071292 June 6, 2000 Makower et al.
6077281 June 20, 2000 Das
6080194 June 27, 2000 Pachence et al.
6083522 July 4, 2000 Chu et al.
6090116 July 18, 2000 Aversa et al.
6113623 September 5, 2000 Sgro
6120539 September 19, 2000 Eldridge et al.
6132765 October 17, 2000 Dicosmo et al.
6143037 November 7, 2000 Goldstein et al.
6153292 November 28, 2000 Bell et al.
6162962 December 19, 2000 Hinsch et al.
6165488 December 26, 2000 Tardy et al.
6171318 January 9, 2001 Kugel et al.
6174320 January 16, 2001 Kugel et al.
6176863 January 23, 2001 Kugel et al.
6179872 January 30, 2001 Bell et al.
6180848 January 30, 2001 Flament et al.
6197325 March 6, 2001 Macphee et al.
6197934 March 6, 2001 Devore et al.
6197935 March 6, 2001 Doillon et al.
6210439 April 3, 2001 Firmin et al.
6214020 April 10, 2001 Mulhauser et al.
6221109 April 24, 2001 Geistlich et al.
6224616 May 1, 2001 Kugel
6241768 June 5, 2001 Agarwal et al.
6258124 July 10, 2001 Darois et al.
6262332 July 17, 2001 Ketharanathan
6264702 July 24, 2001 Ory et al.
6267772 July 31, 2001 Mulhauser et al.
6270530 August 7, 2001 Eldridge et al.
6277397 August 21, 2001 Shimizu
6280453 August 28, 2001 Kugel et al.
6287316 September 11, 2001 Agarwal et al.
6289700 September 18, 2001 Gangi et al.
6290708 September 18, 2001 Kugel et al.
6306079 October 23, 2001 Trabucco
6306424 October 23, 2001 Vyakarnam et al.
6312474 November 6, 2001 Francis et al.
6319264 November 20, 2001 Tormala et al.
6328686 December 11, 2001 Robert
6334872 January 1, 2002 Termin et al.
6383201 May 7, 2002 Dong
6391060 May 21, 2002 Ory et al.
6391333 May 21, 2002 Li et al.
6391939 May 21, 2002 Tayot et al.
6408656 June 25, 2002 Ory et al.
6410044 June 25, 2002 Chudzik et al.
6413742 July 2, 2002 Olsen et al.
6425924 July 30, 2002 Rousseau
6428978 August 6, 2002 Olsen et al.
6436030 August 20, 2002 Rehil
6440167 August 27, 2002 Shimizu
6443964 September 3, 2002 Ory et al.
6447551 September 10, 2002 Goldmann
6447802 September 10, 2002 Sessions et al.
6448378 September 10, 2002 Devore et al.
6451032 September 17, 2002 Ory et al.
6451301 September 17, 2002 Sessions et al.
6454787 September 24, 2002 Maddalo et al.
6477865 November 12, 2002 Matsumoto
6479072 November 12, 2002 Morgan et al.
6485503 November 26, 2002 Jacobs et al.
6500464 December 31, 2002 Ceres et al.
6500777 December 31, 2002 Wiseman et al.
6509031 January 21, 2003 Miller et al.
6511958 January 28, 2003 Atkinson et al.
6514286 February 4, 2003 Leatherbury et al.
6514514 February 4, 2003 Atkinson et al.
6540773 April 1, 2003 Dong
6541023 April 1, 2003 Andre et al.
6548077 April 15, 2003 Gunasekaran
6554855 April 29, 2003 Dong
6559119 May 6, 2003 Burgess et al.
6566345 May 20, 2003 Miller et al.
6575988 June 10, 2003 Rousseau
6576019 June 10, 2003 Atala
6596002 July 22, 2003 Therin et al.
6596304 July 22, 2003 Bayon et al.
6599323 July 29, 2003 Melican et al.
6599524 July 29, 2003 Li et al.
6599690 July 29, 2003 Abraham et al.
6610006 August 26, 2003 Amid et al.
6613348 September 2, 2003 Jain
6616685 September 9, 2003 Rousseau
6623963 September 23, 2003 Mueller et al.
6630414 October 7, 2003 Matsumoto
6637437 October 28, 2003 Hungerford et al.
6638284 October 28, 2003 Rousseau et al.
6645226 November 11, 2003 Jacobs et al.
6652594 November 25, 2003 Francis et al.
6652595 November 25, 2003 Nicolo
6653450 November 25, 2003 Berg et al.
6656206 December 2, 2003 Corcoran et al.
6660280 December 9, 2003 Allard et al.
6669735 December 30, 2003 Pelissier
6670018 December 30, 2003 Fujita et al.
6682760 January 27, 2004 Noff et al.
6685714 February 3, 2004 Rousseau
6706684 March 16, 2004 Bayon et al.
6706690 March 16, 2004 Reich et al.
6712859 March 30, 2004 Rousseau et al.
6719795 April 13, 2004 Bryan et al.
6723335 April 20, 2004 Moehlenbruck et al.
6726660 April 27, 2004 Hessel et al.
6730299 May 4, 2004 Fayot et al.
6736823 May 18, 2004 Darois et al.
6736854 May 18, 2004 Vadurro et al.
6737371 May 18, 2004 Planck et al.
6743435 June 1, 2004 Devore et al.
6746458 June 8, 2004 Cloud
6752834 June 22, 2004 Geistlich et al.
6755868 June 29, 2004 Rousseau
6773723 August 10, 2004 Spiro et al.
6783554 August 31, 2004 Amara et al.
6790213 September 14, 2004 Cherok et al.
6790454 September 14, 2004 Abdul et al.
6800082 October 5, 2004 Rousseau
6833408 December 21, 2004 Sehl et al.
6835336 December 28, 2004 Watt
6852330 February 8, 2005 Bowman et al.
6869938 March 22, 2005 Schwartz et al.
6872227 March 29, 2005 Sump et al.
6893653 May 17, 2005 Abraham et al.
6896904 May 24, 2005 Spiro et al.
6926723 August 9, 2005 Mulhauser et al.
6936276 August 30, 2005 Spiro et al.
6939562 September 6, 2005 Spiro et al.
6949625 September 27, 2005 Fayot
6966918 November 22, 2005 Schuldt-Hempe et al.
6971252 December 6, 2005 Therin et al.
6974679 December 13, 2005 Andre et al.
6974862 December 13, 2005 Ringeisen et al.
6977231 December 20, 2005 Matsuda
6984392 January 10, 2006 Bechert et al.
6988386 January 24, 2006 Okawa et al.
7011688 March 14, 2006 Gryska et al.
7021086 April 4, 2006 Ory et al.
7022358 April 4, 2006 Eckmayer et al.
7025063 April 11, 2006 Snitkin et al.
7041868 May 9, 2006 Greene et al.
7060103 June 13, 2006 Carr et al.
RE39172 July 11, 2006 Bayon et al.
7070558 July 4, 2006 Gellman et al.
7087065 August 8, 2006 Ulmsten et al.
7094261 August 22, 2006 Zotti et al.
7098315 August 29, 2006 Schaufler
7101381 September 5, 2006 Ford et al.
7115220 October 3, 2006 Dubson et al.
7156804 January 2, 2007 Nicolo
7156858 January 2, 2007 Schuldt-Hempe et al.
7175852 February 13, 2007 Simmoteit et al.
7192604 March 20, 2007 Brown et al.
7207962 April 24, 2007 Anand et al.
7214765 May 8, 2007 Ringeisen et al.
7226611 June 5, 2007 Yura et al.
7229453 June 12, 2007 Anderson et al.
7252837 August 7, 2007 Guo et al.
7279177 October 9, 2007 Looney et al.
7331199 February 19, 2008 Ory et al.
7393319 July 1, 2008 Merade et al.
7556598 July 7, 2009 Rao
7594921 September 29, 2009 Browning
7614258 November 10, 2009 Cherok et al.
7615065 November 10, 2009 Priewe et al.
7662169 February 16, 2010 Wittmann
7670380 March 2, 2010 Cauthen, III et al.
7682381 March 23, 2010 Rakos et al.
7709017 May 4, 2010 Tayot et al.
7718556 May 18, 2010 Matsuda et al.
7732354 June 8, 2010 Fricke et al.
7785334 August 31, 2010 Ford et al.
7789888 September 7, 2010 Bartee et al.
7799767 September 21, 2010 Lamberti et al.
7806905 October 5, 2010 Ford et al.
7824420 November 2, 2010 Eldridge et al.
7828854 November 9, 2010 Rousseau et al.
7900484 March 8, 2011 Cherok et al.
7931695 April 26, 2011 Ringeisen
8052759 November 8, 2011 Dupic et al.
8079023 December 13, 2011 Chen
8100924 January 24, 2012 Browning
8123817 February 28, 2012 Intoccia et al.
8142515 March 27, 2012 Therin et al.
8157821 April 17, 2012 Browning
8157822 April 17, 2012 Browning
8182545 May 22, 2012 Cherok et al.
8197837 June 12, 2012 Jamiolkowski et al.
8206632 June 26, 2012 Rousseau et al.
8215310 July 10, 2012 Browning
8317872 November 27, 2012 Adams
8323675 December 4, 2012 Greenawalt
8343232 January 1, 2013 Adzich et al.
8366787 February 5, 2013 Brown et al.
8435307 May 7, 2013 Paul
8470355 June 25, 2013 Skalla et al.
8562633 October 22, 2013 Cully et al.
8574627 November 5, 2013 Martakos et al.
8709094 April 29, 2014 Stad et al.
8734471 May 27, 2014 Deitch
8753360 June 17, 2014 Gleiman et al.
8758800 June 24, 2014 Stopek et al.
8784294 July 22, 2014 Goddard
8814887 August 26, 2014 Walther et al.
8828092 September 9, 2014 Toso et al.
8834864 September 16, 2014 Odar et al.
8846060 September 30, 2014 Archibald et al.
8865215 October 21, 2014 Ladet et al.
8877233 November 4, 2014 Obermiller et al.
8911504 December 16, 2014 Mathisen et al.
8920370 December 30, 2014 Sholev et al.
8956373 February 17, 2015 Ford et al.
8962006 February 24, 2015 Bayon et al.
8968762 March 3, 2015 Ladet et al.
8979935 March 17, 2015 Lozier et al.
9034357 May 19, 2015 Stopek
9113993 August 25, 2015 Lee
9211175 December 15, 2015 Stopek et al.
9216075 December 22, 2015 Bailly et al.
20020087174 July 4, 2002 Capello
20020095218 July 18, 2002 Carr et al.
20030086975 May 8, 2003 Ringeisen
20030106346 June 12, 2003 Matsumoto
20030114937 June 19, 2003 Leatherbury et al.
20030133967 July 17, 2003 Ruszczak et al.
20030225355 December 4, 2003 Butler
20040034373 February 19, 2004 Schuldt-Hempe et al.
20040054376 March 18, 2004 Ory et al.
20040059356 March 25, 2004 Gingras
20040101546 May 27, 2004 Gorman et al.
20050002893 January 6, 2005 Goldmann
20050021058 January 27, 2005 Negro
20050085924 April 21, 2005 Darois et al.
20050113849 May 26, 2005 Popadiuk et al.
20050137512 June 23, 2005 Campbell et al.
20050142161 June 30, 2005 Freeman et al.
20050148963 July 7, 2005 Brennan
20050175659 August 11, 2005 Macomber et al.
20050232979 October 20, 2005 Shoshan
20050267521 December 1, 2005 Forsberg
20050288691 December 29, 2005 Leiboff
20060116696 June 1, 2006 Odermatt et al.
20060135921 June 22, 2006 Wiercinski et al.
20060147501 July 6, 2006 Hillas et al.
20060216320 September 28, 2006 Kitazono et al.
20060252981 November 9, 2006 Matsuda et al.
20060253203 November 9, 2006 Alvarado
20060282103 December 14, 2006 Fricke et al.
20070088391 April 19, 2007 Mcalexander et al.
20070129736 June 7, 2007 Solecki
20070198040 August 23, 2007 Buevich et al.
20070299538 December 27, 2007 Roeber
20080091276 April 17, 2008 Deusch et al.
20080109017 May 8, 2008 Herweck et al.
20080113001 May 15, 2008 Herweck et al.
20080172071 July 17, 2008 Barker
20080255593 October 16, 2008 St-Germain
20090035341 February 5, 2009 Wagener et al.
20090036996 February 5, 2009 Roeber
20090068250 March 12, 2009 Gravagna et al.
20090105526 April 23, 2009 Piroli et al.
20090163936 June 25, 2009 Yang et al.
20090187197 July 23, 2009 Roeber et al.
20090192530 July 30, 2009 Adzich et al.
20090204129 August 13, 2009 Fronio
20090216338 August 27, 2009 Gingras et al.
20090228021 September 10, 2009 Leung
20090270999 October 29, 2009 Brown
20090281558 November 12, 2009 Li et al.
20090318752 December 24, 2009 Evans et al.
20100104608 April 29, 2010 Abuzaina et al.
20100318108 December 16, 2010 Datta et al.
20110015760 January 20, 2011 Kullas
20110022083 January 27, 2011 Dimatteo et al.
20110144667 June 16, 2011 Horton et al.
20110190795 August 4, 2011 Hotter et al.
20110238094 September 29, 2011 Thomas et al.
20110251699 October 13, 2011 Ladet et al.
20110257666 October 20, 2011 Ladet et al.
20110270278 November 3, 2011 Overes et al.
20120016388 January 19, 2012 Houard et al.
20120029537 February 2, 2012 Mortarino
20120065727 March 15, 2012 Reneker et al.
20120082712 April 5, 2012 Stopek et al.
20120116425 May 10, 2012 Intoccia et al.
20120150204 June 14, 2012 Mortarino et al.
20120165937 June 28, 2012 Montanari et al.
20120179175 July 12, 2012 Hammell et al.
20120179176 July 12, 2012 Wilson et al.
20120197415 August 2, 2012 Montanari et al.
20120330093 December 27, 2012 Odermatt et al.
20130172915 July 4, 2013 Thomas et al.
20140044861 February 13, 2014 Boey et al.
20140364684 December 11, 2014 Lecuivre et al.
Foreign Patent Documents
1317836 May 1993 CA
201879864 June 2011 CN
19544162 April 1997 DE
19718903 December 1997 DE
19751733 December 1998 DE
19832634 January 2000 DE
10019604 October 2001 DE
10120942 October 2001 DE
10043396 June 2002 DE
0194192 September 1986 EP
0248544 December 1987 EP
0263360 April 1988 EP
0276890 August 1988 EP
0372969 June 1990 EP
0531742 March 1993 EP
0544485 June 1993 EP
0552576 July 1993 EP
0611561 August 1994 EP
0614650 September 1994 EP
0621014 October 1994 EP
0625891 November 1994 EP
0637452 February 1995 EP
0664132 July 1995 EP
0705878 April 1996 EP
0719527 July 1996 EP
0774240 May 1997 EP
0797962 October 1997 EP
0800791 October 1997 EP
0827724 March 1998 EP
0836838 April 1998 EP
0847727 June 1998 EP
0876808 November 1998 EP
0895762 February 1999 EP
0898944 March 1999 EP
1017415 July 2000 EP
1036545 September 2000 EP
1052319 November 2000 EP
1055757 November 2000 EP
1090590 April 2001 EP
1216717 June 2002 EP
1216718 June 2002 EP
0693523 November 2002 EP
1273312 January 2003 EP
1315468 June 2003 EP
1382728 January 2004 EP
1484070 December 2004 EP
1561480 August 2005 EP
1645232 April 2006 EP
1674048 June 2006 EP
1691606 August 2006 EP
1782848 May 2007 EP
2229918 September 2010 EP
2327373 June 2011 EP
2244853 April 1975 FR
2257262 August 1975 FR
2308349 November 1976 FR
2453231 October 1980 FR
2612392 September 1988 FR
2715309 July 1995 FR
2715405 July 1995 FR
2724563 March 1996 FR
2730406 August 1996 FR
2744906 August 1997 FR
2766698 February 1999 FR
2771622 June 1999 FR
2773057 July 1999 FR
2774277 August 1999 FR
2779937 December 1999 FR
2859624 December 2005 FR
2876020 April 2006 FR
2863277 June 2006 FR
2884706 April 2008 FR
2929834 October 2009 FR
2953709 June 2011 FR
1174814 December 1969 GB
2051153 January 1981 GB
2306110 April 1997 GB
H0332677 March 1991 JP
H05237128 September 1993 JP
H09137380 May 1997 JP
H11146888 June 1999 JP
2008538300 October 2008 JP
2011078767 April 2011 JP
8902445 March 1989 WO
8908467 September 1989 WO
9012551 November 1990 WO
9206639 April 1992 WO
9220349 November 1992 WO
9310731 June 1993 WO
9311805 June 1993 WO
9318174 September 1993 WO
9417747 August 1994 WO
9507666 March 1995 WO
9518638 July 1995 WO
9532687 December 1995 WO
9603091 February 1996 WO
9608277 March 1996 WO
9609795 April 1996 WO
9614805 May 1996 WO
9641588 December 1996 WO
9735533 October 1997 WO
9835632 August 1998 WO
9849967 November 1998 WO
9905990 February 1999 WO
9906079 February 1999 WO
9906080 February 1999 WO
9951163 October 1999 WO
0016821 March 2000 WO
0067663 November 2000 WO
0115625 March 2001 WO
0180773 November 2001 WO
0181667 November 2001 WO
0207648 January 2002 WO
0217853 March 2002 WO
02078568 October 2002 WO
03002168 January 2003 WO
2004004600 January 2004 WO
2004071349 August 2004 WO
2004078120 September 2004 WO
2004103212 December 2004 WO
2005011280 February 2005 WO
2005013863 February 2005 WO
2005018698 March 2005 WO
2005048708 June 2005 WO
2005105172 November 2005 WO
2006018552 February 2006 WO
2006023444 March 2006 WO
2006032812 March 2006 WO
2009071998 June 2009 WO
2009031035 January 2010 WO
2010043978 April 2010 WO
2007048099 September 2010 WO
2011007062 January 2011 WO
2011026987 March 2011 WO
2011038740 April 2011 WO
2013098347 July 2013 WO
Other references
  • Amid, P., “Lichtenstein tension-free hemioplasty: Its inception, evolution, and principles,” Hernia, 2004; pp. 1-7, 8, published online Sep. 2003.
  • Blondin, C. et al., “Inhibition of Complement Activation by Natural Sulfated Polysaccharides (Fucans) from Brown Seaweed,” Molecular Immuol., Mar. 1994, pp. 247-253, 31(4).
  • Blondin, C. et al., “Relationships between chemical characteristics and anticomplementary activity of fucans,” Biomaterials, Mar. 1996, pp. 597-603, 17(6).
  • Boisson-Vidal, C. et al., “Neoangiogenesis Induced by Progenitor Endothelial Cells: Effect of Fucoidan From Marine Algae,” Cardiovascular & Hematological Agents in Medicinal Chem., Jan. 2007, pp. 67-77, 5(1).
  • Bracco, P. et al., “Comparison of polypropylene and polyethylene terephthalate (Dacron) meshes for abdominal wall hernia repair: A chemical and morphological study,” Hernia, 2005, pp. 51-55, 9 (1), published online Sep. 2004.
  • Chen, G. et al., “A Hybrid Network of Synthetic Polymer Mesh and Collagen Sponge,” The Royal Society of Chemistry 2000, Chem. Commun., Jul. 2000, pp. 1505-1506.
  • Collins, R. et al., “Use of collagen film as a dural substitute: Preliminary animal studies,” Journal of Biomedical Materials Research, Feb. 1991, pp. 267-276, vol. 25.
  • D'Dwyer, P. et al., “Randomized clinical trial assessing impact of a lightweight or heavyweight mesh on chronic pain after inguinal hernia repair,” Br. J. Surg., Feb. 2005, pp. 166-170, 92(2).
  • Dr. S. Raz, “The Karl Mayer Guide to Tehnical Textiles,” Jan. 2000, pp. 1-36, Obertshausen, Germany.
  • European Search Report for EP16306383.7 date of completion is May 9, 2017 (4 pages).
  • Haneji, K. et al., “Fucoidan extracted from Cladosiphon Okamuranus Tokida Induces Apoptosis of Human T-cell Leukemia Virus Type 1-Infected T-Cell Lines and Primary Adult T-Cell Leukemia Cells,” Nutrition and Cancer, 2005, pp. 189-201, 52(2), published online Nov. 2009.
  • Haroun-Bouhedja, F. et al., “In Vitro Effects of Fucans on MDA-MB231 Tumor Cell Adhesion and Invasion,” Anticancer Res., Jul.-Aug. 2002, pp. 2285-2292, 22(4).
  • Haroun-Bouhedja, F. et al., “Relationship between sulfate groups and biological activities of fucans,” Thrombosis Res., Dec. 2000, pp. 453-459, 100(5).
  • Hirano, S. et al., “The blood biocompatibility of chitosan and N-acylchitosans,” J. Biomed. Mater. Res., Apr. 1985, 413-417, 19.
  • Junge, K. et al., “Functional and Morphologic Properties of a Modified Mesh for Inguinal Hernia Repair,” World J. Surg., Sep. 2002, pp. 1472-1480, 26.
  • Kanabar, V. et al., “Some structural determinants of the antiproliferative effect of heparin-like molecules on human airway smooth muscle,” Br. J. Pharmacol., Oct. 2005, pp. 370-777, 146(3).
  • Klinge, U. et al., “Foreign Body Reaction to Meshes Used for the Repair of Abdominal Wall Hernias,” Eur J. Surg, Sep. 1999, pp. 665-673, 165.
  • Klinge, U. et al., “Functional and Morphological Evaluation of a Low-Weight, Monofilament Polypropylene Mesh for Hernia Repair,” J Biomed. Mater. Res., Jan. 2002, pp. 129-136, 63.
  • Langenbech, M. R. et al., “Comparison of biomaterials in the early postoperative period,” Surg Endosc., May 2003, pp. 1105-1109, 17 (7).
  • Logeart, D. et al., “Fucans, sulfated polysaccharides extracted from brown seaweeds, inhibit vascular smooth muscle cell proliferation. II. Degradation and molecular weight effect,” Eur. J. Cell. Biol., Dec. 1997, pp. 385-390, 74(4).
  • Machine Translation EP 0 621 014 (Year: 1994).
  • Machine Translation EP 1 382 728 (Year: 2003).
  • Malette, W. G. et al., “Chitosan, A New Hemostatic,” Ann Th. Surg., Jul. 1983, pp. 55-58, 36.
  • Muzzarelli, R. et al., “Reconstruction of parodontal tissue with chitosan,” Biomaterials, Nov. 1989, pp. 598-604, 10.
  • Prokop, A. et al., “Water Soluble Polymers for Immunoisolation I: Complex Coacevation and Cytotoxicity,” Advances in Polymer Science, Jul. 1998, pp. 1-51, 136.
  • Rao, B. et al., “Use of chitosan as a biomaterial: Studies on its safety and hemostatic potential,” J. Biomed. Mater. Res., Jan. 1997, pp. 21-28, 34.
  • Rosen, M. et al., “Laparoscopic component separation in the single-stage treatment of infected abdominal wall prosthetic removal,” Hernia, 2007, pp. 435-440, 11, published online Jul. 2007.
  • Scheidbach, H. et al., “In vivo studies comparing the biocompatibility of various polypropylene meshes and their handling properties during endoscopic total extraperitoneal (TEP) patchplasty: An experimental study in pigs,” Surg. Endosc., Feb. 2004, pp. 211-220, 18(2).
  • Strand, S. et al., “Screening of Chitosans and Conditions for Bacterial Flocculation,” Biomacromolecules, Mar. 2001, 126-133, 2.
  • Varum, K. et al., “In vitro degradation rates of partially N-acetylated chitosans in human serum,” Carbohydrate Research, Mar. 1997, pp. 99-101, 299.
  • Welty, G. et al., “Functional impairment and complaints following incisional hernia repair with different polypropylene meshes,” Hernia, Aug. 2001; pp. 142-147, 5.
  • Zvyagintseva, T. et al., “Inhibition of complement activation by water-soluble polysaccharides of some far-eastern grown seaweeds,” Comparative Biochem and Physiol, Jul. 2000, pp. 209-215,126(3).
Patent History
Patent number: 11696819
Type: Grant
Filed: Jun 15, 2020
Date of Patent: Jul 11, 2023
Patent Publication Number: 20200306024
Assignee: SOFRADIM PRODUCTION (Trevoux)
Inventors: Xavier Couderc (Frans), Pierre Bailly (Caluire-et-Cuire)
Primary Examiner: Timothy J Neal
Assistant Examiner: Andrew P. Restaino
Application Number: 16/902,208
Classifications
Current U.S. Class: Surgical Mesh, Connector, Clip, Clamp Or Band (606/151)
International Classification: D04B 21/12 (20060101); A61F 2/00 (20060101); A61B 17/06 (20060101);